ChemicalBook--->CAS DataBase List--->636-76-0

636-76-0

636-76-0 Structure

636-76-0 Structure
IdentificationBack Directory
[Name]

3-SULFAMOYL-BENZOIC ACID
[CAS]

636-76-0
[Synonyms]

Nsc22977
NSC 85501
BUTTPARK 148\07-55
TIMTEC-BB SBB010997
3-SULFAMOYL-BENZOIC
3-sulfaMoylbenzoate
3-Sulfamoylbenzoicaci
3-Sulfamylbenzoic acid
m-Sulfamoylbenzoic acid
m-Sulfamidobenzoic acid
3-SULFAMOYL-BENZOIC ACID
M-carboxybenzenesulfonamide
3-Sulfamoyl-benzoic acid ,97%
Benzoic acid, 3-(aminosulfonyl)-
[Molecular Formula]

C7H7NO4S
[MDL Number]

MFCD01122318
[MOL File]

636-76-0.mol
[Molecular Weight]

201.2
Chemical PropertiesBack Directory
[Melting point ]

251-252℃
[Boiling point ]

476.1±47.0 °C(Predicted)
[density ]

1.536±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

pK1:3.54 (25°C)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26-24/25-22
[HazardClass ]

IRRITANT
[HS Code ]

29350090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-(Chlorosulfonyl)benzoic acid-->Ammonia
[Preparation Products]

3-Cyanobenzene-1-sulfonyl chloride-->3-cyano-N-ethylbenzene-1-sulfonamide-->3-cyano-N-cyclohexylbenzenesulfonamide-->Benzenesulfonamide, 3-(hydroxymethyl)- (9CI)
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

3-(Chlorosulfonyl)benzoic acid

4025-64-3

3-SULFAMOYL-BENZOIC ACID

636-76-0

General procedure for the synthesis of 3-sulfobenzoic acid from 3-chlorosulfonylbenzoic acid: 25 g of 3-(chlorosulfonyl)benzoic acid (commercially available, Aldrich) was added in batches to 250 mL of 25% ammonium hydroxide solution under ice bath conditions. The reaction mixture was stirred at room temperature for 15 hours. Upon completion of the reaction, the solvent was concentrated by distillation under reduced pressure to about 50 mL. Subsequently, the mixture was acidified with concentrated hydrochloric acid to pH < 2. The precipitated white solid was collected by filtration and dried with a vacuum desiccator to afford 22 g (96% yield) of 3-sulfobenzoic acid. The product was characterized as follows: 1H NMR (DMSO-d6) δ 13.44 (br s, 1H), 8.38 (s, 1H), 8.14 (d, J = 7.5 Hz, 1H), 8.04 (d, J = 7.9 Hz, 1H), 7.72 (t, J = 7.9 Hz, 1H), 7.49 (s, 2H); HPLC (max plot) 97%; Rt 0.68 min; LC/MS (ES-): 199.8.

[References]

[1] Patent: WO2007/23186, 2007, A1. Location in patent: Page/Page column 45
[2] European Journal of Medicinal Chemistry, 2014, vol. 89, p. 503 - 523
[3] Journal of the American Chemical Society, 2011, vol. 133, # 40, p. 16235 - 16242
[4] ChemMedChem, 2015, vol. 10, # 9, p. 1548 - 1558
[5] Patent: US2013/35364, 2013, A1. Location in patent: Paragraph 0233-0235
Spectrum DetailBack Directory
[Spectrum Detail]

3-SULFAMOYL-BENZOIC ACID(636-76-0)1HNMR
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