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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
22 Results for "
Suzuki coupling reaction
" in MedChemExpress (MCE) Product Catalog:
Products (22)
22 Results for "Suzuki coupling reaction" in MCE Product Catalog:
Cat. No.: HY-21623
CAS No.: 95464-05-4
Cat. No.: HY-W002570
CAS No.: 32316-92-0
Cat. No.: HY-W003601
CAS No.: 357927-50-5
Cat. No.: HY-32959
CAS No.: 135884-31-0
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-32927
CAS No.: 150255-96-2
Target:
Research Areas:
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-32956
CAS No.: 163105-90-6
Target:
Research Areas:
2-Methoxypyridine-3-boronic acid is a pyridine boronic acid compound and also borylation reagent used in Suzuki cross-coupling reactions .
Cat. No.: HY-101974
CAS No.: 1041766-91-9
Target:
Research Areas:
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-171854
CAS No.: 3040121-49-8
Target:
Research Areas:
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 .
Cat. No.: HY-W020940
CAS No.: 12012-95-2
Target:
Research Areas:
Allylpalladium(II) chloride dimer is a palladium catalytic precursor that serves as a catalyst for the Heck reaction. Allylpalladium(II) chloride dimer is also a transition metal allyl complex .
Cat. No.: HY-32928
CAS No.: 126747-14-6
Target:
Research Areas:
4-Cyanobenzeneboronic acid is a boronic acid derivative and also coupling reagent in Suzuki cross-coupling reactions .
Cat. No.: HY-W004698
CAS No.: 628692-15-9
Cat. No.: HY-77642
CAS No.: 149104-88-1
Cat. No.: HY-W002463
CAS No.: 63503-60-6
Cat. No.: HY-206852
CAS No.: 2055777-51-8
Research Areas:
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 .
Cat. No.: HY-W020985
CAS No.: 31277-98-2
Synonyms: Pd(DIPHOS)2
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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
