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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, 5-amino-

Nc1ccc2c(c1)cc(s2)C(=O)O Request for Quotation
Chemical Name: Benzo[b]thiophene-2-carboxylic acid, 5-amino-
CAS Number: 98589-46-9
Product Number: AG0067DW(AGN-PC-0KKQBE)
Synonyms:
MDL No:
Molecular Formula: C9H7NO2S
Molecular Weight: 193.2224

Identification/Properties

Properties
MP:
274-276℃
BP:
467.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
193.22g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
193.02g/mol
Monoisotopic Mass:
193.02g/mol
Topological Polar Surface Area:
91.6A^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#:
-
Hazard Statements:
H335-H319-H315
Precautionary Statements:
P271-P261-P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Aminobenzo[b]thiophene-2-carboxylic acid is a versatile compound that finds widespread use in chemical synthesis processes. Primarily utilized as a building block in organic chemistry, this compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 5-Aminobenzo[b]thiophene-2-carboxylic acid acts as a valuable precursor in the creation of complex organic molecules. Its functional groups allow for strategic manipulation through different chemical reactions, facilitating the generation of diverse derivatives with tunable properties. This compound is particularly valued for its ability to introduce the benzo[b]thiophene moiety into target molecules, imparting desired characteristics and functionalities.Furthermore, the conjugated structure of 5-Aminobenzo[b]thiophene-2-carboxylic acid enables its incorporation into aromatic systems, enabling the development of advanced materials with specific electronic and optical properties. Its presence can enhance the stability, reactivity, or bioactivity of the final products, making it a crucial component in the design and synthesis of novel compounds for various applications.Overall, 5-Aminobenzo[b]thiophene-2-carboxylic acid is a valuable tool in the hands of chemists, enabling the synthesis of complex molecules with tailored properties for pharmaceutical, agricultural, and materials science applications.