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Results for "

Suzuki Coupling

" in MedChemExpress (MCE) Product Catalog:

26

Inhibitors & Agonists

1

Fluorescent Dyes

17

Biochemical Assay Reagents

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-21623
    Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct

    		Biochemical Assay Reagents Others
    Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl2, a phosphine ligand palladium(II) complex, which can be used as a versatile precatalyst for various cross-coupling reactions. Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct can stabilize reaction intermediates and lower the reaction activation energy in coupling reactions, and can be used in Suzuki-Miyaura coupling reaction studies .
    Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct
  • HY-114362
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate

    TPGS-750-M

    		 Biochemical Assay Reagents Others
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate (TPGS-750-M) is an amphiphile, acts as a surfactant. DL-alpha-Tocopherol methoxypolyethylene glycol succinate has a positive effect on Suzuki-Miyaura cross coupling. DL-alpha-Tocopherol methoxypolyethylene glycol succinate increases the styrene titer. DL-alpha-Tocopherol methoxypolyethylene glycol succinate is used in the stability test of NPYM-modified drugs in biological fluids .
    DL-alpha-Tocopherol methoxypolyethylene glycol succinate
  • HY-40249
    1-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester

    		Drug Intermediate Others
    1-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester is a drug intermediate that can be used for the preparation of SMARCA bromodomain ligands .
    1-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester
  • HY-Y0747
    Iodobenzene

    1-Iodobenzene

    		 Biochemical Assay Reagents Others
    Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl .
    Iodobenzene
  • HY-W002570
    2-Naphthylboronic acid

    		Biochemical Assay Reagents Others
    2-Naphthylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Naphthylboronic acid can undergo silylation reaction. 2-Naphthylboronic acid also readily undergo Suzuki-Miyaura cross-coupling .
    2-Naphthylboronic acid
  • HY-W003601
    2-Bromo-4-fluoropyridine

    		Biochemical Assay Reagents Others
    2-Bromo-4-fluoropyridine is a synthetic halogenated heterocyclic organic compound and a key intermediate in the pharmaceutical and agrochemical industries. 2-Bromo-4-fluoropyridine can be used to synthesize bioactive molecules through cross-coupling reactions, such as Suzuki coupling or Buchwald-Hartwig amination.
    2-Bromo-4-fluoropyridine
  • HY-32748
    2-Bromo-5-fluoropyridine

    		Biochemical Assay Reagents Drug Intermediate Others
    2-Bromo-5-fluoropyridine is an intermediate. 2-Bromo-5-fluoropyridine can undergo Suzuki coupling reaction with Boronic acid (HY-41551). 2-Bromo-5-fluoropyridine can be used in the synthesis of GSK1292263A (a GPR119 receptor agonist) .
    2-Bromo-5-fluoropyridine
  • HY-75129
    Pyridin-3-ylboronic acid

    		Biochemical Assay Reagents Others
    Pyridin-3-ylboronic acid is an organic compound. Pyridin-3-ylboronic acid is a key reagent in the Suzuki-Miyaura cross-coupling reaction. Pyridin-3-ylboronic acid is used in organic synthesis to construct oligopyridine compounds, and then as an α-helix mimetic to study protein-protein interactions .
    Pyridin-3-ylboronic acid
  • HY-W003129
    2-Bromo-4-chloropyridine

    		Drug Intermediate Bacterial Infection
    2-Bromo-4-chloropyridine is a halogenated pyridine derivative that serves as a synthetic intermediate. 2-Bromo-4-chloropyridine undergoes Suzuki-Miyaura coupling with 4-tert-butylphenylboronic acid (HY-W007389). 2-Bromo-4-chloropyridine facilitates the construction of compounds with broad-spectrum antibacterial activity .
    2-Bromo-4-chloropyridine
  • HY-32959
    N-Boc-2-pyrroleboronic acid

    		Biochemical Assay Reagents Others
    N-Boc-2-pyrroleboronic acid is an organic synthesis intermediate used primarily in the synthesis of chiral pharmaceutical molecules and biologically active molecules. The boronic acid on the pyrrole ring can participate in Suzuki coupling reactions. The boronic acid can be oxidized to a hydroxyl group under the action of nitrogen oxides, and after tautomerization, it can be further transformed into 2-oxo-2,5-dihydro-1-pyrrolecarboxylic acid tert-butyl ester .
    N-Boc-2-pyrroleboronic acid
  • HY-75637
    3-Amino-5-methylpyrazole

    		Drug Intermediate Others
    5-Methyl-1H-pyrazol-3-amine is a pyrazole heterocyclic compound and can be used as a key intermediate for the synthesis of pyrazolylamide derivatives.
    3-Amino-5-methylpyrazole
  • HY-101974
    Biotin-PEG3-Bromide

    		Biochemical Assay Reagents Others
    Biotin-PEG3-Bromide is a short PEG linker featuring a biotin group and a bromide. The bromide is a halogen which is easily displaced by nucleophiles such as alcohols or amines. Alternatively, bromide can be applied in a number of cross-coupling reactions such as in a Suzuki reaction. Biotin is useful for affinity-based applications such as pull-down assays or for ligating with streptavidin proteins.
    Biotin-PEG3-Bromide
  • HY-Y0747S
    Iodobenzene-d5

    1-Iodobenzene-d5

    		 Isotope-Labeled Compounds Others
    Iodobenzene-d5 is the deuterium labeled 1-Iodobenzene. Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl .
    Iodobenzene-d5
  • HY-W002801
    2-Benzyloxyphenylboronic acid

    		Biochemical Assay Reagents Others
    2-Benzyloxyphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Benzyloxyphenylboronic acid is also a substrate used in asymmetric Suzuki coupling reactions. 2-Benzyloxyphenylboronic acid can be utilized in the synthesis of other active compounds .
    2-Benzyloxyphenylboronic acid
  • HY-171854
    SB-583355

    		G2A (GPR132) Neurological Disease Inflammation/Immunology
    SB-583355 (Compound 56) is a potent G2A antagonist. SB-583355 can be prepared by a Suzuki reaction between 4-methoxyphenyl boronic acid and 3-bromo-4-hydroxybenzoic acid following the conditions followed by an amide coupling reaction. SB-583355 blocks the activation of G2A mediated either by 9-HOPE or T-10148 in human G2A expressing CHO-K1 cells. SB-583355 can be studied in research for inflammation, myeloid leukemia, and neuropathic pain .
    SB-583355
  • HY-20176
    2,4-Dichlorothieno[3,2-d]pyrimidine

    		Drug Intermediate Adenosine Receptor PI3K Infection
    2,4-Dichlorothieno[3,2-d]pyrimidine is a thienopyrimidine scaffold and a key synthetic precursor, which is widely used for constructing 4-arylthieno[3,2-d]pyrimidine compounds. 2,4-Dichlorothieno[3,2-d]pyrimidine serves for the development of 4-arylthieno[3,2-d]pyrimidine-based human adenosine A2a receptor antagonists, as well as thienopyrimidine-based PI3K-α inhibitors. In addition, 2,4-Dichlorothieno[3,2-d]pyrimidine has potential application value in studies related to whipworm disease .
    2,4-Dichlorothieno[3,2-d]pyrimidine
  • HY-32928
    4-Cyanobenzeneboronic acid

    		Biochemical Assay Reagents Others
    4-Cyanobenzeneboronic acid is a Boronic acid derivative. 4-Cyanobenzeneboronic acid can be used in Suzuki-Miyaura cross-coupling reactions .
    4-Cyanobenzeneboronic acid
  • 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-W004698
    (2-Methoxypyrimidin-5-yl)boronic acid

    		Drug Intermediate Others
    (2-Methoxypyrimidin-5-yl)boronic acid is a drug intermediate that can serve as a key reactant in the Suzuki-Miyaura coupling reaction, and is used for the synthesis of isoquinoline ketone derivatives with anti-tumor activity .
    (2-Methoxypyrimidin-5-yl)boronic acid
  • HY-77642
    4-(Methylsulfonyl)phenylboronic acid

    		Biochemical Assay Reagents Drug Intermediate Metabolic Disease
    4-(Methylsulfonyl)phenylboronic acid is an intermediate. 4-(Methylsulfonyl)phenylboronic acid can be used to synthesize GPR119 agonists via Suzuki coupling reaction. 4-(Methylsulfonyl)phenylboronic acid can be used in the research of type 2 diabetes .
    4-(Methylsulfonyl)phenylboronic acid
  • HY-206852
    PF-06445974 precursor

    		Drug Intermediate Phosphodiesterase (PDE) Neurological Disease
    PF-06445974 precursor (Compound 28) is a nitro precursor and synthetic intermediate. PF-06445974 precursor can be used for the synthesis of PF-06445974 (HY-119190). PF-06445974 is a positron emission tomography (PET) compound that acts potently on PDE4B .
    PF-06445974 precursor
  • HY-W002463
    3-Chlorophenyl boronic acid

    		Biochemical Assay Reagents Others
    3-Chlorophenylboronic acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. 3-Chlorophenylboronic acid is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors among others. 3-Chlorophenyl boronic acid can affect cell migration. 3-Chlorophenyl boronic acid can be used to study wound healing .
    3-Chlorophenyl boronic acid
  • 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)
  • HY-W019633
    Benzothiazole-5-boronic acid pinacol ester

    		Biochemical Assay Reagents Others
    Benzothiazole-5-boronic acid pinacol ester is a compound that can be used in the boronate part of Suzuki coupling reactions .
    Benzothiazole-5-boronic acid pinacol ester
  • HY-W005558
    6-Aminopyridine-3-boronic acid

    		Biochemical Assay Reagents Others
    6-Aminopyridine-3-boronic acid is a boronic acid derivative. Boronic acid derivatives are widely used in organic synthesis for carbon-carbon bond formation. In Suzuki coupling, aryl halides and boronic acid aryl or vinyl esters or boronic acid are coupled using Pd(PPh3)4. It can be used as a pharmaceutical intermediate [1] .
    6-Aminopyridine-3-boronic acid
  • HY-Y0747S1
    Iodobenzene-d2

    1-Iodobenzene-d2

    		 Isotope-Labeled Compounds Others
    Iodobenzene-d2 is the deuterium labeled 1-Iodobenzene. Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl .
    Iodobenzene-d2

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