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6961-82-6

Basic Information
CAS No.: 6961-82-6
Name: o-Chlorobenzenesulfonamide
Article Data: 24
Cas Database
Molecular Structure:
Molecular Structure of 6961-82-6 (o-Chlorobenzenesulfonamide)
Formula: C6H6ClNO2S
Molecular Weight: 191.638
Synonyms: Benzenesulfonamide,o-chloro- (6CI,8CI);2-Chlorobenzenesulfonamide;2-Chlorophenylsulfonamide;A 4097;NSC 62927;
EINECS: 230-156-7
Density: 1.47 g/cm3
Melting Point: 189-193 °C(lit.)
Boiling Point: 352.9 °C at 760 mmHg
Flash Point: 167.2 °C
Solubility: 498.3mg/L(15 oC)
Appearance: slight yellow powder
Hazard Symbols: IrritantXi
Risk Codes: 36/37/38
Safety: 26-36
Transport Information: N/A
PSA: 68.54000
LogP: 2.76850
Synthetic route
2905-23-9

2-chlorophenylsulfonyl chloride

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With ammonium hydroxide In tetrahydrofuran at 0 - 20℃; for 2.16667h;99.1%
With ammonium hydroxide In tetrahydrofuran at 0 - 20℃; for 2.16667h;99.1%
With ammonium hydroxide In tetrahydrofuran at 0 - 20℃; for 2.16667h;99.1%

2-(2-chlorobenzenesulfonylamino)-2-methylpropionic acid

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With oxygen; copper(II) oxide In dimethyl sulfoxide at 100℃; for 8h;89%
5183-78-8

methyl(phenylsulfonyl)amide

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With N-chloro-succinimide; silver hexafluoroantimonate; trifluorormethanesulfonic acid; nickel diacetate In 1,2-dichloro-ethane at 80℃; for 12h; regioselective reaction;71%
1956-97-4

2-chlorobenzenediazonium tetrafluoroborate

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With sodium metabisulfite; sodium azide; tetrabutylammomium bromide; triphenylphosphine In water; acetonitrile at 80℃; for 12h; Inert atmosphere;62%
With sodium metabisulfite; sodium azide; tetrabutylammomium bromide; triphenylphosphine In water; acetonitrile at 80℃; for 12h; Inert atmosphere; Schlenk technique;62%
64900-65-8

2-chlorophenylsulfonyl isocyanate

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With Methamphetamin In dichloromethane for 0.5h; Yield given;
95-51-2

2-Chloroaniline

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
Sandmeyer reaction;
Multi-step reaction with 2 steps
1: 1) NaNO2, 20percent H2SO4 2) CuCl2*2H2O, SO2 / 1) H2O, 15 - 20 deg C, 15 min 2) AcOH, HCl, benzene, 30 - 40 deg C
2: 86.5 percent / 25percent NH2OH*H2O / 1)
View Scheme
64902-72-3

1-(2-chlorophenylsulfonyl)-3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)urea

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With hydrogenchloride In methanol at 50℃; for 4h; Hydrolysis;

(o-Chlorophenylsulfonyl)carbamic acid

A

124-38-9

carbon dioxide

B

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With phosphoric acid In various solvent(s) at 25℃; pH=2.80; Kinetics; Activation energy; Further Variations:; pH-values; Solvents; Temperatures; Reagents; Hydrolysis;
2-chloro-benzene-sulfonyl chloride-(1)

2-chloro-benzene-sulfonyl chloride-(1)

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
With ammonia; water
17315-42-3

(CH3)3SnC6H4-o-Cl

6961-82-6

2-chlorobenzenesulfonamide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: CH2Cl2 / 15 h / 20 °C
2: ice / CH2Cl2 / 0.5 h
View Scheme
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    o-Chlorobenzenesulfonamide Basic information Product Name: o-Chlorobenzenesulfonamide Synonyms: 2-chloro-benzenedulfonamid;Benzenesulfonamide, 2-chloro-;Benzenesulfonamide, o-chloro-;2-CHLOROBENZENESULPHONAMIDE;2-CHLOROBENZENESULFONAMIDE;BUTTP

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    o-Chlorobenzenesulfonamide

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  • o-Chlorobenzenesulfonamide CAS No.6961-82-6

  • Casno:

    6961-82-6

    o-Chlorobenzenesulfonamide CAS No.6961-82-6

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    2-Chlorobenzenesulfonamide

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    2-Chlorobenzenesulfonamide

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    Hangzhou Keying Chem Co., Ltd. Is a comprehensive enterprise, dedicated to the development, production and marketing of chemicals. As a technology innovative and service professional enterprise, Our company mainly engages in global pharmaceutical, ch

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     China (Mainland)  |  Contact Details

    Business Type:Lab/Research institutions

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