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Home > Encyclopedia > 3-Aminobenzenesulfonamide

3-Aminobenzenesulfonamide

3-Aminobenzenesulfonamide structure

3-Aminobenzenesulfonamide 

structure
  • CAS No:

    98-18-0

  • Formula:

    C6H8N2O2S

  • Chemical Name:

    3-Aminobenzenesulfonamide

  • Synonyms:

    Benzenesulfonamide,3-amino-;Metanilamide;3-Aminobenzenesulfonamide;m-Aminobenzenesulfonamide;3-Aminosulfonylaniline;m-Sulfamoylaniline;NSC 7542;3-Sulfamoylaniline;3-Sulfamoylphenylamine;3-Aminobenzene-1-sulfonamide;4431-73-6

  • Categories:

    Active Pharmaceutical Ingredients  >  Synthetic Anti-infective Drugs

Description

Deep yellow powder

3-Aminobenzenesulfonamide Basic Attributes

172.20500

172.20

202-646-0

7542

DTXSID5059161

2935009090

Characteristics

94.56000

-0.4

1.427 g/cm3

139-141 °C

420.7ºC at 760 mmHg

208.3ºC

1.627

11.96g/L(24 ºC)

Safety Information

NONH for all modes of transport

3

R36/37/38

S24/25

OY2200000

Xi

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3-Aminobenzenesulfonamide Use and Manufacturing

Methods of Manufacturing

(a) 3-aminobenzenesulfonamide b. Synthesis of 3-amino-benzenesulfonamide.; 3-Nitro-benzenesulfonamide (1.46 g, 7.2 mmol) was hydrogenated over Raney nickel (0.3 g) in methanol at 50Take 8a (558mg, 3mmol) was dissolved in absolute ethanol (30.0 mL of), the The addition of stannous chloride (5.0 equiv.) Was carried out at 70 °C for 6 h, TLC was monitored until the reaction was complete, cooled to room temperature, With 5percent sodium bicarbonate solution to adjust the pH to 9-10, A large amount of yellow floc appears in the system, extracted with ethyl acetate, The organic phase was washed with saturated brine, the organic phase was separated, Dried over anhydrous sodium sulfate, filtered to obtain a filtrate, the organic reagent was distilled off, A yellow oil was added thereto, ethyl acetate was added thereto, The petroleum ether regulates the polarity of the system, and a large amount of solid appears. The yellow powder is filtered 9a (210mg, 41.7percent).

Uses

Used as an intermediate in organic synthesis.

Benzenesulfonamide, 3-amino-: INACTIVE

Computed Properties

Molecular Weight:172.21
XLogP3:-0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:172.03064868
Monoisotopic Mass:172.03064868
Topological Polar Surface Area:94.6
Heavy Atom Count:11
Complexity:219
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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