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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Thiazole-5-boronic acid

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Chemical Name: Thiazole-5-boronic acid
CAS Number: 942190-81-0
Product Number: AG00IHZJ(AGN-PC-0WAJQ5)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


Thiazol-5-ylboronic acid is a versatile chemical compound that finds widespread application in organic synthesis. As a boronic acid derivative, it serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and materials. In chemical synthesis, Thiazol-5-ylboronic acid acts as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This allows for the efficient assembly of complex organic molecules, making it an essential tool for medicinal chemists and researchers working in drug discovery and development. Additionally, Thiazol-5-ylboronic acid can also participate in other important transformations such as metal-catalyzed C-H activation reactions, making it a versatile and valuable reagent in modern synthetic organic chemistry.