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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, 3-[[(4-methoxyphenyl)amino]sulfonyl]-

COc1ccc(cc1)NS(=O)(=O)c1cccc(c1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 3-[[(4-methoxyphenyl)amino]sulfonyl]-
CAS Number: 147410-81-9
Product Number: AG019GIM(AGN-PC-0JW46E)
Synonyms:
MDL No:
Molecular Formula: C14H13NO5S
Molecular Weight: 307.3217

Identification/Properties

Computed Properties
Molecular Weight:
307.32g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
307.051g/mol
Monoisotopic Mass:
307.051g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
451
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


3-[(4-methoxyphenyl)sulfamoyl]benzoic acid is a versatile compound widely utilized in chemical synthesis. Its primary application lies in organic chemistry as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials.One prominent usage of 3-[(4-methoxyphenyl)sulfamoyl]benzoic acid is in the synthesis of sulfonamides, a class of compounds known for their antibacterial properties. By utilizing this compound as a precursor, chemists can efficiently introduce the sulfonamide functional group into target molecules, enhancing their biological activity and specificity.Additionally, this compound serves as a valuable intermediate in the preparation of dyes, pigments, and photoactive materials. Its unique structure allows for the introduction of diverse functionalities, enabling the synthesis of compounds with tailored properties for various industrial applications.In the field of medicinal chemistry, 3-[(4-methoxyphenyl)sulfamoyl]benzoic acid is often employed in the development of novel drug candidates. Its sulfonamide moiety offers potential interactions with biological targets, making it a valuable scaffold for the design of new therapeutic agents with improved efficacy and safety profiles.Overall, the versatility and reactivity of 3-[(4-methoxyphenyl)sulfamoyl]benzoic acid make it an indispensable tool for chemists engaged in the synthesis of complex molecules with diverse applications in the pharmaceutical, agrochemical, and materials science industries.