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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)-

3-bromo-5-phenylthiophene-2-carboxylic acid

OC(=O)c1sc(cc1Br)c1ccccc1 Request for Quotation
Chemical Name: 3-bromo-5-phenylthiophene-2-carboxylic acid
CAS Number: 1017687-42-1
Product Number: AG0005FL(AGN-PC-03NRSR)
Synonyms:
MDL No:
Molecular Formula: C11H7BrO2S
Molecular Weight: 283.1411

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromo-5-phenylthiophene-2-carboxylic acid is a versatile compound that finds wide application in organic chemical synthesis. Its unique structure and reactivity make it a valuable building block for the construction of complex organic molecules. One of the primary uses of this compound is in the preparation of heterocyclic compounds, which are essential in the pharmaceutical industry for drug discovery and development. Additionally, 3-Bromo-5-phenylthiophene-2-carboxylic acid can be utilized in the synthesis of agrochemicals, materials science, and other specialty chemicals. Its ability to undergo various chemical transformations, such as coupling reactions and functional group manipulations, makes it a valuable tool for organic chemists in designing and creating novel molecules with diverse applications.