Dipropyl disulfide
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; potassium nitrate In dichloromethane at 50℃; for 4h; | 98% |
propyl thiocyanate
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With water; chlorine at 5℃; | |
Stage #1: propyl thiocyanate With water; acetic acid at 50℃; for 0.5h; Stage #2: With sulfuryl dichloride at 50℃; for 0.5h; | |
With water; chlorine at 5℃; |
Conditions | Yield |
---|---|
With tetrachloromethane; sulfur dioxide; chlorine Irradiation.mit UV-Licht; |
propanesulfonic acid
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With phosphorus pentachloride | |
With sulfuryl dichloride In N,N-dimethyl-formamide at 100 - 105℃; for 3h; Yield given; | |
With triethylamine In acetone at 80℃; for 0.333333h; microwave irradiation; |
1-thiopropane
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With chlorine; acetic acid |
dipropyl sulfoxide
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With water; chlorine In water at 25 - 30℃; for 1.5h; |
propyl bromide
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
(i) aq. (NH4)2SO3, (ii) PCl5; Multistep reaction; |
1-propanesulfonic acid sodium salt
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With chlorine-triphenylphosphine In acetonitrile for 15h; Ambient temperature; |
propyl thiocyanate
water
chlorine
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
Natrium-Salz reagiert; |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With phosphorus pentachloride |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With phosphorus pentachloride |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With water; chlorine at 10 - 15℃; |
n-propanesulfonyl chloride
propane-1-sulfonamide
Conditions | Yield |
---|---|
With ammonia In diethyl ether at 0℃; for 0.166667h; | 100% |
With ammonia In toluene at -78℃; for 1h; | 83.1% |
With ammonia In tetrahydrofuran at 20℃; for 0.3h; | 59.5% |
n-propanesulfonyl chloride
benzotriazol-1-ol
1-hydroxybenzotriazol propanesulfonate
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane at 0℃; for 1h; | 100% |
n-propanesulfonyl chloride
1-(3-aminophenyl)ethanone
N-(3-acetylphenyl)-1-propane-sulfonamide
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; for 20h; | 100% |
n-propanesulfonyl chloride
4-cyano-4-phenylpiperidine hydrochloride
4-phenyl-1-(propylsulfonyl)piperidine-4-carbonitrile
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 2h; | 100% |
n-propanesulfonyl chloride
1-t-Butoxycarbonylpiperazine
tert-butyl 4-(propylsulfonyl)piperazine-1-carboxylate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 25℃; for 3h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; | 90% |
With triethylamine In dichloromethane | |
With triethylamine In tert-butyl methyl ether at 20℃; for 2h; | 13.5 g |
n-propanesulfonyl chloride
4-Methyl-3-nitroanilin
N-(4-methyl-3-nitrophenyl)-N-(propylsulfonyl)propane-1-sulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 2h; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
n-propanesulfonyl chloride
3,4-dihydroxy-2,5-dicarboxylic acid thiophene
Conditions | Yield |
---|---|
Stage #1: 3,4-dihydroxy-2,5-dicarboxylic acid thiophene With pyridine at 5 - 25℃; for 1h; Inert atmosphere; Stage #2: n-propanesulfonyl chloride With triethylamine at 7 - 25℃; for 18h; Inert atmosphere; | 100% |
n-propanesulfonyl chloride
tert-butyl (4-aminobenzyl)carbamate
tert-butyl N-[(4-propylsulfonylamino)benzyl]carbamate
Conditions | Yield |
---|---|
With pyridine at 20℃; for 16h; | 99% |
With pyridine In dichloromethane at 20℃; |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
In pyridine | 99% |
N-cyclohexyl-1-(2,4-dichlorophenyl)-5-(4-hydroxyphenyl)-4-methyl-1H-pyrazole-3-carboxamide
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 99% |
n-propanesulfonyl chloride
3-Hydroxyacetophenone
3-acetylphenyl propane-1-sulfonate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 5h; | 99% |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 99% |
With pyridine In dichloromethane at 20℃; | 47% |
4-cyanopiperidine
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 2.5h; | 99% |
n-propanesulfonyl chloride
4-bromo-2-methoxyaniline
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; for 16h; Inert atmosphere; | 99% |
With pyridine In dichloromethane at 20℃; for 16h; Inert atmosphere; | 99% |
1-(2,4-dichlorophenyl)-5-(4-hydroxyphenyl)-1H-pyrazole-3-carboxylic acid ethyl ester
n-propanesulfonyl chloride
1-(2,4-dichlorophenyl)-5-[4-(propane-1-sulfonyloxy)-phenyl]-1H-pyrazole-3-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 1h; | 98% |
With triethylamine In dichloromethane at 0℃; for 1h; | 98% |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3h; | 98% |
2-amino-3,4-difluoronitro-benzene
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
Stage #1: 2-amino-3,4-difluoronitro-benzene With sodium hydride In tetrahydrofuran; mineral oil at 20℃; for 0.5h; Stage #2: n-propanesulfonyl chloride In tetrahydrofuran; mineral oil at 20℃; | 98% |
n-propanesulfonyl chloride
sodium propane-1-sulfinate
Conditions | Yield |
---|---|
With sodium carbonate; sodium sulfite In water for 1h; Reflux; | 97% |
With sodium hydrogencarbonate; sodium sulfite In water at 80℃; for 4h; | 87% |
With sodium carbonate; sodium sulfite In water at 80℃; for 1h; | |
With sodium hydrogencarbonate; sodium sulfite In water at 80℃; for 4h; |
n-propanesulfonyl chloride
(4S,5S)-4-(biphenyl-4-yl)-2,2-dimethyl-1,3-dioxan-5-amine
N-[(4S,5S)-4-(biphenyl-4-yl)-2,2-dimethyl-1,3-dioxan-5-yl]propane-1-sulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; | 97% |
With triethylamine In dichloromethane for 2h; 0 deg C to r.t.; |
n-propanesulfonyl chloride
methyl 2-chloro-3-amino-6-fluorobenzoate
methyl 2-chloro-6-fluoro-3-(propylsulfonamido)benzoate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3.33333h; | 97% |
With triethylamine In dichloromethane at 20℃; for 2h; | 97% |
Stage #1: methyl 3-amino-2-chloro-6-fluorobenzoate With triethylamine In dichloromethane at 0℃; for 1.33333h; Stage #2: n-propanesulfonyl chloride In dichloromethane at 20℃; for 2h; | 97% |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 3h; | 97% |
2,4-dichloro-3-iodoaniline
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 1h; | 97% |
n-propanesulfonyl chloride
(6-aminospiro[3.3]hept-2-yl)carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 97% |
n-propanesulfonyl chloride
1,1-difluoro-2-(2-naphthyl)ethene
Conditions | Yield |
---|---|
Stage #1: n-propanesulfonyl chloride With sodium hydrogencarbonate; sodium sulfite In water at 80℃; for 12h; Inert atmosphere; Stage #2: 1,1-difluoro-2-(2-naphthyl)ethene In dimethyl sulfoxide at 40℃; for 48h; Inert atmosphere; | 97% |
n-propanesulfonyl chloride
benzylamine
N-benzylpropane-1-sulfonamide
Conditions | Yield |
---|---|
In ethyl acetate at 0 - 20℃; for 1h; | 96% |
In tetrahydrofuran at 0 - 20℃; | 89% |
With triethylamine In acetonitrile at 0 - 20℃; Yield given; |
furan-2-ylmethanamine
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With dmap; triethylamine In tetrahydrofuran a) 0 deg C, 3 h, b) RT, 12 h; | 96% |
n-propanesulfonyl chloride
5-bromo-2-methylaniline
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane at 20℃; for 16h; | 96% |
With pyridine; dmap In dichloromethane at 20℃; for 40h; Inert atmosphere; | 96% |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 3h; | 96% |
n-propanesulfonyl chloride
Conditions | Yield |
---|---|
With sodium hydroxide In 2-methyltetrahydrofuran; water at 10 - 20℃; pH=2; | 96% |
IUPAC Name: Propane-1-sulfonyl chloride
Systematic of 1-Propanesulfonyl chloride (CAS NO.10147-36-1): EINECS 233-414-7 ; Propanesulphonyl chloride
CAS NO: 10147-36-1
Molecular Formula of 1-Propanesulfonyl chloride (CAS NO.10147-36-1): C3H7ClO2S
Molecular Weight: 142.6045
Molecular Structure:
H bond acceptors: 2
Freely Rotating Bonds: 2
Polar Surface Area: 42.52 Å2
Index of Refraction: 1.448
Molar Refractivity: 29.58 cm3
Molar Volume: 110.4 cm3
Surface Tension: 37.3 dyne/cm
Density of 1-Propanesulfonyl chloride (CAS NO.10147-36-1): 1.29 g/cm3
Flash Point: 64.9 °C
Enthalpy of Vaporization: 41.13 kJ/mol
Boiling Point: 192.6 °C at 760 mmHg
Vapour Pressure: 0.675 mmHg at 25°C
Hazard Codes: C
Risk Statements: 14-34-36
R14: Reacts violently with water.
R34: Causes burns.
R36: Irritating to eyes.
Safety Statements: 26-36/37/39-45
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection.
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: UN 3265 8/PG 2
WGK Germany: 3
F: 10-19-21
HazardClass: 8
PackingGroup: III
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