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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, chloro-

OC(=O)c1sccc1Cl Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, chloro-
CAS Number: 59337-89-2
Product Number: AG0038M2(AGN-PC-0JV55Q)
Synonyms:
MDL No: MFCD00043888
Molecular Formula: C5H3ClO2S
Molecular Weight: 162.5941

Identification/Properties

Computed Properties
Molecular Weight:
162.587g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
161.954g/mol
Monoisotopic Mass:
161.954g/mol
Topological Polar Surface Area:
65.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
128
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chlorothiophene-2-carboxylic acid is a versatile compound that finds wide application in chemical synthesis. One of its key uses is as a building block in the synthesis of pharmaceuticals and agrochemicals. This compound serves as a valuable precursor in the creation of various biologically active molecules due to its unique structure and reactivity. Additionally, 3-Chlorothiophene-2-carboxylic acid is employed in the development of specialty chemicals, such as dyes and organic materials. Its incorporation into diverse chemical reactions enables the formation of complex molecular structures with specific properties, making it a valuable tool in the realm of organic synthesis.