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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)-

Benzo[b]thiophene-2-carboxylic acid, 6-fluoro-

Fc1ccc2c(c1)sc(c2)C(=O)O Request for Quotation
Chemical Name: Benzo[b]thiophene-2-carboxylic acid, 6-fluoro-
CAS Number: 142329-23-5
Product Number: AG007YU1(AGN-PC-0LK94Y)
Synonyms:
MDL No:
Molecular Formula: C9H5FO2S
Molecular Weight: 196.1982

Identification/Properties

Computed Properties
Molecular Weight:
196.195g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
195.999g/mol
Monoisotopic Mass:
195.999g/mol
Topological Polar Surface Area:
65.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
222
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:
H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Fluorobenzo[b]thiophene-2-carboxylic acid is a versatile chemical compound commonly utilized in organic synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, 6-Fluorobenzo[b]thiophene-2-carboxylic acid can be employed as a key intermediate for the preparation of important heterocyclic compounds. Its fluorine substituent imparts specific electronic and steric effects, influencing the overall properties of the final products. Additionally, the carboxylic acid functional group present in the molecule enables facile derivatization for further modification and functionalization.By incorporating 6-Fluorobenzo[b]thiophene-2-carboxylic acid into synthetic routes, chemists can access a diverse array of target molecules with enhanced biological activities, improved solubility, and tailored physicochemical properties. Its strategic placement within a synthetic pathway can lead to the development of novel compounds with potential applications in drug discovery, material science, and crop protection.Overall, the strategic utilization of 6-Fluorobenzo[b]thiophene-2-carboxylic acid in chemical synthesis underscores its significance as a valuable tool for the construction of complex molecules with specific functionalities and desired properties.