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Results for "

cross coupling

" in MedChemExpress (MCE) Product Catalog:

36

Inhibitors & Agonists

22

Biochemical Assay Reagents

1

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-114362
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate

    TPGS-750-M

    		 Biochemical Assay Reagents Others
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate solution (TPGS-750-M) is an amphiphile, acts as a surfactant. DL-alpha-Tocopherol methoxypolyethylene glycol succinate solution has a positive effect on Suzuki-Miyaura cross coupling .
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate
  • HY-161541
    Estradiol/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    Estradiol/BSA is the antigen-adjuvant conjugate formed by the coupling of Estradiol (HY-B0141) with Bovine Serum Albumin (BSA). By coupling the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Estradiol/BSA
  • HY-161562
    PROMETON/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    PROMETON/BSA is an antigen-adjuvant conjugate formed by the coupling of PROMETON with bovine serum albumin (BSA). By coupling the antigen to the protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the production of antigen-specific T cells.
    PROMETON/BSA
  • HY-161530
    Angiotensin II/BSA

    		Angiotensin Receptor Inflammation/Immunology
    Angiotensin II/BSA is an antigen-adjuvant conjugate formed by the coupling of Angiotensin II with bovine serum albumin (BSA). By coupling the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Angiotensin II/BSA
  • HY-W001987
    4,6-Dichloropyrimidin-5-amine

    		Biochemical Assay Reagents Others
    Organic ligands can be prepared through Suzuki cross-coupling reaction between 4,6-Dichloropyrimidin-5-amine and dimethyl(5-pinyl)isophthalate .
    4,6-Dichloropyrimidin-5-amine
  • HY-161589
    GABA/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    GABA/KLH is an antigen-adjuvant conjugate formed by the coupling of GABA (γ-aminobutyric acid) with keyhole limpet hemocyanin (KLH). By coupling the antigen with a protein adjuvant, it can enhance the production of antigen-specific antibodies in vaccine models. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    GABA/KLH
  • HY-161588
    GABA/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    GABA/BSA is an antigen-adjuvant conjugate formed by the coupling of GABA (γ-aminobutyric acid) with Bovine Serum Albumin (BSA). By coupling the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    GABA/BSA
  • HY-W543082
    P(o-tol)3 Pd G2 ChemBeads

    		Others Others
    P(o-tol)3 Pd G2 ChemBeads is a robust and air-stable catalyst featuring a bulky, electron-rich dialkylbiaryl phosphine, specifically designed for Pd-catalyzed cross-coupling reactions.
    P(o-tol)3 Pd G2 ChemBeads
  • HY-120286
    K-13

    		Others Others
    K-13 is a cyclic peptide compound synthesized by a specific organozinc reagent. Its synthesis process involves intermolecular and intramolecular Negishi cross-coupling reactions and is one of the shortest routes reported for the synthesis of such cyclic peptides.
    K-13
  • HY-161526
    T3/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    T3/KLH is an antigen-adjuvant conjugate formed by the coupling of T3 (thyroid hormone) with keyhole limpet hemocyanin (KLH). By coupling the antigen with the protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    T3/KLH
  • HY-W075745
    SK-J003-1n

    		Others
    SK-J003-1n is a nickel catalyst with excellent cross-coupling reaction activity. SK-J003-1n can be used as a ligand in organic synthesis to improve the selectivity and efficiency of the reaction. SK-J003-1n can effectively catalyze the coupling reaction between different substrates, highlighting its important role in compound development and material science.
    SK-J003-1n
  • HY-W034801
    Copper(II) acetylacetonate

    Cupric Acetylacetonate

    		 Biochemical Assay Reagents Others
    Copper(II) acetylacetonate (Cupric Acetylacetonate) is the homoleptic acetylacetonate complex of copper(II). Copper(II) acetylacetonate is used as a catalyst in various organic reactions, including oxidation, cross-coupling, and polymerization reactions. Copper(II) acetylacetonate is also a precursor for making metal-organic frameworks (MOF) and nanomaterials .
    Copper(II) acetylacetonate
  • HY-161561
    PROMETON/OVA

    		Biochemical Assay Reagents Inflammation/Immunology
    PROMETON/OVA is an antigen-adjuvant conjugate formed by the coupling of PROMETON and ovalbumin (OVA). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes and enhances cross-presentation and the production of antigen-specific T cells.
    PROMETON/OVA
  • HY-W033277
    Tetrakis(acetonitrile)palladium(II) tetrafluoroborate

    NSC 307191; Palladium(II) tetrafluoroborate tetraacetonitrile complex

    		 Others Others
    Tetrakis(acetonitrile)palladium(II) tetrafluoroborate (NSC 307191) acts as a potent Lewis acid and facilitates the formation of the 2:1 complex [Pd(1,2-bis(2′-pyridylethynyl)benzene)2](BF4)2 through the Sonogashira cross-coupling reaction.
    Tetrakis(acetonitrile)palladium(II) tetrafluoroborate
  • HY-161549
    Phosphotyrosine/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    Phosphotyrosine/BSA is an antigen-adjuvant conjugate formed by coupling Phosphotyrosine with Bovine Serum Albumin (BSA). By conjugating the antigen with protein adjuvants, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Phosphotyrosine/BSA
  • HY-161566
    DHT/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    DHT/BSA is an antigen-adjuvant conjugate formed by the coupling of DHT (dihydrotestosterone) and bovine serum albumin (BSA). By conjugating the antigen with the protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    DHT/BSA
  • HY-163555
    BZO/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    BZO/BSA is an antigen-adjuvant conjugate formed by the coupling of BZO (benzodiazepine) with bovine serum albumin (BSA). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the production of antigen-specific T cells.
    BZO/BSA
  • HY-161540
    Oxytetracycline/OVA

    		Biochemical Assay Reagents Inflammation/Immunology
    Oxytetracycline/OVA is an antigen-adjuvant conjugate formed by the coupling of Oxytetracycline (HY-B0275) with ovalbumin (OVA). By conjugating the antigen with a protein adjuvant, it enhances the production of antigen-specific antibodies in vaccine models. The conjugate does not affect protein folding or destroy the major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Oxytetracycline/OVA
  • HY-P2890
    Laccase, Microorganisms

    Denilite IIS

    		 Endogenous Metabolite Others
    Laccase, Microorganisms (Denilite IIS) is a multi-copper oxidase (MCOs), which widely exists in microorganisms, plants and fungi, and can catalyze the oxidation of one electron of various phenolic compounds. Laccase can promote the oxidative coupling of single lignin, which plays an important role in the formation and biodegradation of lignin, and also has the potential to cross-link food polymers .
    Laccase, Microorganisms
  • HY-161559
    Sudan I/OVA

    		Biochemical Assay Reagents Inflammation/Immunology
    Sudan I/OVA is an antigen-adjuvant conjugate formed by coupling Sudan I (HY-D0024) with Ovalbumin (OVA). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt the main epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Sudan I/OVA
  • HY-161585
    Diethylstilbestrol/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    Diethylstilbestrol/KLH is an antigen-adjuvant conjugate formed by the coupling of Diethylstilbestrol (HY-14598) with Keyhole Limpet Hemocyanin (KLH). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Diethylstilbestrol/KLH
  • HY-161535
    Oxytetracycline/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    Oxytetracycline/BSA is an antigen-adjuvant conjugate formed by the coupling of Oxytetracycline (HY-B0275) with Bovine Serum Albumin (BSA). By conjugating the antigen with the protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the production of antigen-specific T cells.
    Oxytetracycline/BSA
  • HY-161586
    Chloramphenicol/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    Chloramphenicol/BSA is the antigen-adjuvant conjugate formed by the coupling of Chloramphenicol (HY-B0239) with Bovine Serum Albumin (BSA). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Chloramphenicol/BSA
  • HY-161546
    Melamine/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    Melamine/KLH is an antigen-adjuvant conjugate formed by coupling Melamine (HY-Y1117) with Keyhole Limpet Hemocyanin (KLH). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt the primary epitopes, and can enhance cross-presentation and the generation of antigen-specific T cells.
    Melamine/KLH
  • HY-W075747
    SK-J014-1n

    		Others
    SK-J014-1n is a nickel catalyst with high cross-coupling activity. SK-J014-1n can effectively promote organic synthesis reactions and increase reaction rate and selectivity. SK-J014-1n exhibits good catalytic performance in the synthesis of complex organic molecules.
    SK-J014-1n
  • HY-W543065
    CPhos Pd G2

    		Endogenous Metabolite
    CPhos Pd G2 is a highly efficient palladium catalyst with excellent cross-coupling reaction activity. CPhos Pd G2 is widely used in compound synthesis and material science, especially for the construction of complex organic molecules and the synthesis of bioactive compounds. CPhos Pd G2 is also favored for improving reaction selectivity and reducing the formation of by-products.
    CPhos Pd G2
  • HY-161556
    Alginic acid/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    Alginic acid/KLH is an antigen-adjuvant conjugate formed by the coupling of Alginic acid (HY-W127758) with Keyhole Limpet Hemocyanin (KLH). By conjugating the antigen with the protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Alginic acid/KLH
  • HY-161584
    Sudan I/KLH

    		Biochemical Assay Reagents Inflammation/Immunology
    Sudan I/KLH is an antigen-adjuvant conjugate formed by the coupling of Sudan I (HY-D0024) with Keyhole Limpet Hemocyanin (KLH). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or disrupt major epitopes, and it can enhance cross-presentation and the generation of antigen-specific T cells.
    Sudan I/KLH
  • HY-161565
    Gastrin(1-17)/BSA

    		Biochemical Assay Reagents Inflammation/Immunology
    Gastrin(1-17)/BSA is an antigen-adjuvant conjugate formed by the coupling of Gastrin(1-17) and Bovine Serum Albumin (BSA). By conjugating the antigen with a protein adjuvant, the production of antigen-specific antibodies in vaccine models can be enhanced. The conjugate does not affect protein folding or destroy major epitopes, and it can enhance cross-presentation and the production of antigen-specific T cells.
    Gastrin(1-17)/BSA
  • HY-W583317
    sSPhos Pd G2

    		Endogenous Metabolite
    sSPhos Pd G2 is a palladium catalyst with excellent cross-coupling reaction activity. sSPhos Pd G2 exhibits efficient catalytic ability in the synthesis of organic molecules and compounds. sSPhos Pd G2 can effectively promote the formation of CC bonds, optimize reaction conditions and increase yields. sSPhos Pd G2 is also used in a variety of transformation reactions, helping researchers develop new materials and compounds.
    sSPhos Pd G2
  • HY-W008658
    [1,4-Bis(diphenylphosphino)butane](norbornadiene)rhodium tetrafluoroborate

    		Others
    [1,4-Bis(diphenylphosphino)butane](norbornadiene)rhodium tetrafluoroborate is a highly efficient and selective transition metal catalyst that can catalyze a variety of reactions, including cross-coupling reactions and hydrogenation reactions. This compound is widely used in organic synthesis and helps to promote the development of new compounds and materials. Through its catalytic activity, [1,4-Bis(diphenylphosphino)butane](norbornadiene)rhodium tetrafluoroborate offers the potential to optimize reaction conditions and improve yields.
    [1,4-Bis(diphenylphosphino)butane](norbornadiene)rhodium tetrafluoroborate
  • HY-Y1738
    Tetrakis(triphenylphosphine)palladium

    Tetrakis(triphenylphosphine)palladium(0)

    		 Biochemical Assay Reagents Others
    Tetrakis(triphenylphosphine)palladium (Pd(PPhs)) series of cross-coupling catalysts can be used to construct an organic heterojunction solar cell model. Adding different amounts of Pd(PPhs) significantly affected free carrier generation, non-twin trap and surface trap-assisted recombination as well as bimolecular recombination and charge extraction, but the impact on the non-duplex recombination process was limited because the catalyst could not promote efficient Trap-assisted reorganization. The studied system is highly robust with the addition of a small amount of Pd(PPha) .
    Tetrakis(triphenylphosphine)palladium
  • HY-W034606
    2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole

    CM-Phos

    		 Others
    2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole (CM-Phos) is an organic compound with catalytic activity. 2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole can be used as an efficient catalyst for cross-coupling reactions of various alcohols and olefins. 2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole shows important application potential in pharmaceutical and material science.
    2-[2-(Dicyclohexylphosphino)phenyl]-1-methyl-1H-indole
  • HY-W075744
    SK-J002-1n

    		Others
    SK-J002-1n is a highly efficient catalyst with excellent cross-coupling reaction activity. SK-J002-1n is widely used in organic synthesis to construct complex molecular structures. The chiral properties of SK-J002-1n make it play an important role in the pharmaceutical industry and provide support for the synthesis of chiral compounds. SK-J002-1n can significantly improve the conversion efficiency and is an important component of transition metal catalysts.
    SK-J002-1n
  • HY-W582827
    RuPhos Pd G1 methyl t-butyl ether adduct (MTBE)

    		Others
    RuPhos Pd G1 methyl t-butyl ether adduct (MTBE) is a highly efficient catalyst with excellent cross-coupling activity. RuPhos Pd G1 methyl t-butyl ether adduct (MTBE) is widely used in organic synthesis and can be used to promote various reactions to build complex molecular structures. RuPhos Pd G1 methyl t-butyl ether adduct (MTBE) has good adaptability to temperature and reaction conditions, which enables it to exhibit excellent catalytic performance in different reaction systems.
    RuPhos Pd G1 methyl t-butyl ether adduct (MTBE)
  • HY-W020985
    Bis[1,2-bis(diphenylphosphino)ethane]palladium(0)

    Pd(DIPHOS)2

    		 Biochemical Assay Reagents Others
    Bis[1,2-bis(diphenylphosphino)ethane]palladium(0), often abbreviated as Pd(PPh3)2 or Pd(dppf), is an organometallic compound. This compound is widely used as a catalyst for organic chemical reactions, especially cross-coupling reactions such as Suzuki-Miyaura reaction and Heck reaction, and its high catalytic activity, selectivity and stability make it a versatile tool for the synthesis of complex organic compounds , in addition, the potential application of Pd(PPh3)2 in the production of electronic materials and in medical and biochemical research has also been investigated.
    Bis[1,2-bis(diphenylphosphino)ethane]palladium(0)

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