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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)-

2-Thiophenecarboxylic acid, 4-(hydroxymethyl)-

OCc1csc(c1)C(=O)O Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 4-(hydroxymethyl)-
CAS Number: 14282-65-6
Product Number: AG006XHM(AGN-PC-01MO2K)
Synonyms:
MDL No:
Molecular Formula: C6H6O3S
Molecular Weight: 158.1750

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Chemical Structure


4-(Hydroxymethyl)thiophene-2-carboxylic acid is a versatile compound that finds wide applications in chemical synthesis. With its unique molecular structure, this compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, 4-(Hydroxymethyl)thiophene-2-carboxylic acid serves as a key building block for the creation of complex molecules through reactions such as esterification, amidation, and Suzuki-Miyaura coupling. Additionally, its hydroxyl and carboxylic acid functional groups allow for easy manipulation and derivatization, enabling chemists to tailor its properties for specific applications. This compound's presence in chemical synthesis highlights its significance in the development of new compounds and materials with diverse functionalities and potential industrial applications.