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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)-

Benzoic acid, 2-[(2-aminophenyl)thio]-

OC(=O)c1ccccc1Sc1ccccc1N Request for Quotation
Chemical Name: Benzoic acid, 2-[(2-aminophenyl)thio]-
CAS Number: 54920-98-8
Product Number: AG00DEAC(AGN-PC-0NDGCQ)
Synonyms:
MDL No:
Molecular Formula: C13H11NO2S
Molecular Weight: 245.2969

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


The application of 2-((2-Aminophenyl)thio)benzoic acid in chemical synthesis lies in its ability to serve as a versatile building block for the creation of various organic compounds. With its unique structure containing an aminophenyl group attached to a thioether functional group on a benzoic acid backbone, this compound can participate in a range of synthetic reactions to produce diverse products.In organic synthesis, 2-((2-Aminophenyl)thio)benzoic acid can be utilized as a precursor for the synthesis of pharmaceuticals, agrochemicals, and materials. Its functional groups can undergo chemical transformations such as acylation, amidation, and substitution reactions to introduce different substituents and modifications. This flexibility allows chemists to tailor the molecule for specific applications, enhancing its potential in drug discovery and material science.Furthermore, the thioether group in 2-((2-Aminophenyl)thio)benzoic acid can participate in cross-coupling reactions to form carbon-sulfur bonds, which are important in the construction of complex organic structures. This compound's unique combination of aromatic, amino, and thioether functionalities provides a valuable platform for designing and synthesizing novel molecules with diverse properties and functions.