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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
35 Results for "
Suzuki
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "Suzuki" in MCE Product Catalog:
Cat. No.: HY-21623
CAS No.: 95464-05-4
Cat. No.: HY-W007432
CAS No.: 787618-22-8
Synonyms: TPGS-750-M
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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 .
Cat. No.: HY-W002570
CAS No.: 32316-92-0
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Pyridin-3-ylboronic acid is a synthetic building block belonging to the pyridine boronic acid class. Pyridin-3-ylboronic acid serves as a substrate for the Suzuki-Miyaura coupling reaction to construct oligopyridine backbones. Pyridin-3-ylboronic acid also acts as a heteroaryl boronic acid in the phosphine-free Suzuki-Miyaura coupling reaction of 2-iodogalactal. Pyridin-3-ylboronic acid is applicable to research related to organic synthesis .
Cat. No.: HY-W002465
CAS No.: 5570-19-4
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2-Nitrophenylboronic acid is a small-molecule arylboronic acid reagent selective for cysteine residues that mediates nickel (II)-promoted arylation of cysteine thiols. 2-Nitrophenylboronic acid is used in research related to peptide modification and also serves as a substrate for Suzuki-Miyaura coupling reactions in research related to organic synthesis .
Cat. No.: HY-W003129
CAS No.: 22918-01-0
Cat. No.: HY-32959
CAS No.: 135884-31-0
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4-Fluorobenzeneboronic acid (P-Fluorophenylboronic acid) is a fluorinated arylboronic acid coupling ligand and precursor. Under the catalysis of heterogeneous palladium nanoparticles, 4-Fluorobenzeneboronic acid participates in the Suzuki-Miyaura C-C coupling reaction to generate fluorinated biphenyl derivatives. 4-Fluorobenzeneboronic acid also participates in the copper-catalyzed three-component reaction with nitrobenzene and potassium metabisulfite as substrates, and finally produces sulfonamides through the formation of arylsulfinate intermediates, copper-assisted S-N bond construction and reduction steps .
Cat. No.: HY-78494
CAS No.: 13922-41-3
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1-Naphthaleneboronic acid is a biochemical reagent that can serve as a starting material or reaction reagent for chemical synthesis. 1-Naphthaleneboronic acid mainly introduces its naphthalene ring into other scaffolds through Suzuki-Miyaura cross-coupling or Friedel-Crafts alkylation reactions, thereby synthesizing target products with specific functions such as fluorescence imaging, photodynamic therapy targeting, or affinity adsorption. 1-Naphthaleneboronic acid can be used in research on photosensitizers and the synthesis of hypercrosslinked polymers with boronic acid affinity .
Cat. No.: HY-32748
CAS No.: 41404-58-4
Research Areas:
2-Bromo-5-fluoropyridine acts as a bromofluoropyridine starting material and an azaaryl halide coupling partner. 2-Bromo-5-fluoropyridine participates in an oxygen-promoted, ligand-free Pd (OAc)2-catalyzed Suzuki reaction, reacting with arylboronic acids to produce 5-fluoro-2-aryl-substituted pyridine derivatives. 2-Bromo-5-fluoropyridine can be used to synthesize 5-fluoro-2-(4-(methylsulfonyl) phenyl) pyridine, an intermediate of the GPR119 agonist GSK1292263A .
Cat. No.: HY-32956
CAS No.: 163105-90-6
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2-Methoxypyridine-3-boronic acid is a pyridine boronic acid compound and also borylation reagent used in Suzuki cross-coupling reactions .
Cat. No.: HY-32927
CAS No.: 150255-96-2
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3-Cyanophenylboronic acid is an arylboronic acid-based boronic acid reagent that serves as a coupling partner in Suzuki-Miyaura cross-coupling reactions. 3-Cyanophenylboronic acid participates in reactions to synthesize 4'-propoxybiphenyl-3-carbonitrile .
Cat. No.: HY-101974
CAS No.: 1041766-91-9
Cat. No.: HY-42045
CAS No.: 321724-19-0
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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 .
Cat. No.: HY-W002801
CAS No.: 190661-29-1
Cat. No.: HY-W583317
CAS No.: 2375242-78-5
Research Areas:
sSPhos Pd G2 is a water-soluble palladium catalyst. sSPhos Pd G2 mediates Suzuki-Miyaura cross-coupling reactions for protein biotinylation and on-DNA reactions, thereby enabling robust gel-based ABPP using iodocysteine-reactive probes rather than bromo- or chloro-substituted probes .
Cat. No.: HY-171854
CAS No.: 3040121-49-8
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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 .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
