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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, 3-hydroxy-, ethyl ester

CCOC(=O)c1sccc1O Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 3-hydroxy-, ethyl ester
CAS Number: 2158-88-5
Product Number: AG007PWD(AGN-PC-0JLP4T)
Synonyms:
MDL No:
Molecular Formula: C7H8O3S
Molecular Weight: 172.2016

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Chemical Structure


Ethyl 3-hydroxythiophene-2-carboxylate plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows for various synthetic transformations, making it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and functional materials. With its hydroxyl and carboxylic acid functionalities, this compound can participate in diverse reactions such as esterification, amidation, and coupling reactions. Additionally, the thiophene ring offers aromatic properties that can be exploited in the design of novel compounds with desired physical and chemical properties. In the realm of chemical synthesis, Ethyl 3-hydroxythiophene-2-carboxylate serves as a key component for creating complex molecular structures and driving innovation in the development of new substances with potential applications across various industries.