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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)-

3-[methyl(propan-2-yl)sulfamoyl]benzoic acid

CC(N(S(=O)(=O)c1cccc(c1)C(=O)O)C)C Request for Quotation
Chemical Name: 3-[methyl(propan-2-yl)sulfamoyl]benzoic acid
CAS Number: 747411-03-6
Product Number: AG00ICJZ(AGN-PC-0KC64L)
Synonyms:
MDL No: MFCD05270845
Molecular Formula: C11H15NO4S
Molecular Weight: 257.3061

Identification/Properties

Computed Properties
Molecular Weight:
257.304g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
257.072g/mol
Monoisotopic Mass:
257.072g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
371
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


The compound, 3-[Methyl(propan-2-yl)sulfamoyl]benzoic Acid, is a versatile building block used in chemical synthesis for its unique reactivity and functional groups. It serves as a key intermediate in the creation of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, this compound can be employed as a key starting material for the production of sulfonamides, which are essential components in many pharmaceuticals due to their antimicrobial and anti-inflammatory properties. Its sulfamoyl group can undergo various reactions, such as substitution and elimination, to introduce diverse functionalities into the molecule.Furthermore, the presence of the benzoic acid moiety in this compound allows for further modifications through different chemical transformations, enabling the creation of structurally diverse molecules for various applications in the fields of medicinal chemistry and material science.Overall, the 3-[Methyl(propan-2-yl)sulfamoyl]benzoic Acid plays a crucial role in chemical synthesis by providing a versatile platform for the construction of complex and biologically active compounds.