3-Aminobenzenesulfonamide

  • CasNo:98-18-0
  • purity:99%
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Details

Factory Sells Best Quality 3-Aminobenzenesulfonamide 98-18-0 with stock

  • Molecular Formula: C6H8N2O2S
  • Molecular Weight: 172.208
  • Vapor Pressure: 2.75E-07mmHg at 25°C 
  • Melting Point: 139 °C 
  • Refractive Index: 1.627 
  • Boiling Point: 420.7 °C at 760 mmHg 
  • PKA: 10.34±0.60(Predicted) 
  • Flash Point: 208.3 °C 
  • PSA: 94.56000 
  • Density: 1.427 g/cm3 
  • LogP: 2.27850 

3-Aminobenzenesulfonamide(Cas 98-18-0) Usage

InChI:InChI=1/C6H8N2O2S/c7-5-2-1-3-6(4-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)

98-18-0 Relevant articles

-

Kumler,Halverstadt

, p. 2182,2187 (1941)

-

Selective Reduction of Nitroarenes to Arylamines by the Cooperative Action of Methylhydrazine and a Tris(N-heterocyclic thioamidate) Cobalt(III) Complex

Ioannou, Dimitris I.,Gioftsidou, Dimitra K.,Tsina, Vasiliki E.,Kallitsakis, Michael G.,Hatzidimitriou, Antonios G.,Terzidis, Michael A.,Angaridis, Panagiotis A.,Lykakis, Ioannis N.

, p. 2895 - 2906 (2021/02/27)

We report an efficient catalytic protoco...

Preparation of Well-Ordered Mesoporous-Silica-Supported Ruthenium Nanoparticles for Highly Selective Reduction of Functionalized Nitroarenes through Transfer Hydrogenation

Wei, Ning,Zou, Xiujing,Huang, Haigen,Wang, Xueguang,Ding, Weizhong,Lu, Xionggang

supporting information, p. 209 - 214 (2018/01/26)

MCM-41-type mesoporous silica (OMS-IL) w...

N,N'-bis-substituted aryl thiourea derivatives and synthetic method and application thereof

-

Paragraph 0069-0071, (2017/04/26)

The invention discloses N,N'-bis-substit...

Discovery of a Series of 5,11-Dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-ones as Selective PI3K-δ/γ Inhibitors

Ferguson, Fleur M.,Ni, Jing,Zhang, Tinghu,Tesar, Bethany,Sim, Taebo,Kim, Nam Doo,Deng, Xianming,Brown, Jennifer R.,Zhao, Jean J.,Gray, Nathanael S.

, p. 908 - 912 (2016/10/22)

Dual inhibition of PI3K-δ and PI3K-γ is ...

98-18-0 Process route

3-nitrobenzenesulphonyl chloride
121-51-7

3-nitrobenzenesulphonyl chloride

m-aminobenzenesulfonamide
98-18-0

m-aminobenzenesulfonamide

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: 40 percent / NH3 ; TEA; DMAP / tetrahydrofuran / 20 °C
2: 80 percent / Fe; NH4 Cl / ethanol; H2 O / 3 h / 90 °C
With dmap; TEA; ammonia; iron; ammonium chloride; In tetrahydrofuran; ethanol; water;
Multi-step reaction with 2 steps
1: ammonia; triethylamine / dichloromethane / 20 °C
2: hydrogen; palladium on activated charcoal / methanol / 20 °C
With palladium on activated charcoal; ammonia; hydrogen; triethylamine; In methanol; dichloromethane;
Multi-step reaction with 2 steps
1: ammonia; ammonium carbonate / water; acetonitrile / 1 h / 20 °C
2: hydrogen / nickel / methanol / 4 h / 50 °C / 3620.13 Torr
With ammonia; hydrogen; ammonium carbonate; nickel; In methanol; water; acetonitrile;
m-aminobenzenesulfonamide
98-18-0

m-aminobenzenesulfonamide

Conditions
Conditions Yield
With hydrogenchloride; tin;

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