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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-[(dimethylamino)sulfonyl]-4-fluoro-

Fc1ccc(cc1S(=O)(=O)N(C)C)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 3-[(dimethylamino)sulfonyl]-4-fluoro-
CAS Number: 381229-72-7
Product Number: AG019VCI(AGN-PC-0NG6MC)
Synonyms:
MDL No:
Molecular Formula: C9H10FNO4S
Molecular Weight: 247.2434

Identification/Properties

Computed Properties
Molecular Weight:
247.24g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
247.031g/mol
Monoisotopic Mass:
247.031g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
362
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


With its unique structure, 3-(Dimethylsulfamoyl)-4-fluorobenzoic Acid serves as a versatile building block in chemical synthesis. Its enhanced stability and reactivity make it an ideal reagent for the creation of novel compounds in pharmaceutical, agrochemical, and material science research. As a key intermediate in organic synthesis, this compound facilitates the formation of complex molecular structures through efficient functional group transformations and selective reactions. Additionally, its compatibility with a variety of reaction conditions allows for the precise manipulation of chemical bonds, enabling the synthesis of diverse chemical entities with tailored properties and functionalities. Furthermore, the presence of the dimethylsulfamoyl and fluorobenzoic moieties imparts specific characteristics to the synthesized compounds, making them valuable tools in the development of new drugs, materials, and molecular probes.