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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, 5-(aminosulfonyl)-2-chloro-

OC(=O)c1cc(ccc1Cl)S(=O)(=O)N Request for Quotation
Chemical Name: Benzoic acid, 5-(aminosulfonyl)-2-chloro-
CAS Number: 97-04-1
Product Number: AG00IJVZ(AGN-PC-0JL7EE)
Synonyms:
MDL No:
Molecular Formula: C7H6ClNO4S
Molecular Weight: 235.6448

Identification/Properties

Computed Properties
Molecular Weight:
235.638g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
234.971g/mol
Monoisotopic Mass:
234.971g/mol
Topological Polar Surface Area:
106A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
323
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Aminosulfonyl)-2-chlorobenzoic acid is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its sulfonamide group provides a valuable handle for introducing specificity and enhancing biological activity in drug design. In organic synthesis, 5-(Aminosulfonyl)-2-chlorobenzoic acid can be utilized as a precursor for the preparation of diverse heterocyclic compounds and functional materials through various synthetic routes such as amide bond formation, Suzuki-Miyaura coupling, and Heck reactions. Its chlorine substituent offers opportunities for selective functionalization and diversification, making it an indispensable tool in the toolbox of synthetic chemists. Additionally, the presence of an amino group in the molecule enables further derivatization to modulate its physicochemical properties and introduce desired functionalities into target molecules. Overall, the strategic incorporation of 5-(Aminosulfonyl)-2-chlorobenzoic acid in chemical synthesis unlocks a plethora of possibilities for the efficient construction of complex structures with tailored properties for diverse applications.