4-n-propylbenzenesulfonyl chloride

Names

[ CAS No. ]:
146949-07-7

[ Name ]:
4-n-propylbenzenesulfonyl chloride

[Synonym ]:
4-propylbenzenesulfonyl chloride
4-Propylbenzene-1-sulfonyl chloride
MFCD00041508

Chemical & Physical Properties

[ Density]:
1.223

[ Boiling Point ]:
275-276ºC

[ Melting Point ]:
21ºC

[ Molecular Formula ]:
C₉H₁₁ClO₂S

[ Molecular Weight ]:
218.70000

[ Flash Point ]:
108ºC

[ Exact Mass ]:
218.01700

[ PSA ]:
42.52000

[ LogP ]:
3.64740

[ Vapour Pressure ]:
0.00287mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.5400(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3265 8/PG 2

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ HS Code ]:
2904909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Association of hydrotropes in aqueous solution studied by reaction kinetics. Buurma NJ, et al.

Adv. Synth. Catal. 344(3/4) , 413-420, (2002)

Synthesis, characterization and catalytic properties of novel palladium (II) complexes containing aromatic sulfonamides: effective catalysts for the oxidation of benzyl alcohol. Dayan S and Kalaycioglu NO.

Appl. Organomet. Chem. 27(1) , 52-58, (2013)

4-n-propylbenzenesulfonyl chloride
4-n-propylbenzoyl chloride
4-n-Pentylbenzoyl chloride
4-n-hexyloxybenzoyl chloride
4-Decylbenzoyl chloride
4-N-NONYLBENZOYL CHLORIDE
ethyl 5-amino-4-(2-methoxyethyl)-1-methyl-1H-pyrazole-3-carboxylate
2-methyl-5-(propan-2-yl)-4,5,6,7-tetrahydro-2H-indazol-3-amine
(1R,2S)-2-{[(4-{[(tert-butoxy)carbonyl]amino}cyclohexyl)({[(9H-fluoren-9-yl)methoxy]carbonyl})amino]methyl}cyclopropane-1-carboxylic acid
5-({[(1R,3R)-3-{[(tert-butoxy)carbonyl]amino}cyclohexyl]({[(9H-fluoren-9-yl)methoxy]carbonyl})amino}methyl)-1-methyl-1H-pyrrole-2-carboxylic acid
5-({[(3R,4R)-1-[(tert-butoxy)carbonyl]-4-methoxypyrrolidin-3-yl]({[(9H-fluoren-9-yl)methoxy]carbonyl})amino}methyl)-1,2-dimethyl-1H-pyrrole-3-carboxylic acid
4-[({1-[(tert-butoxy)carbonyl]pyrrolidin-3-yl}({[(9H-fluoren-9-yl)methoxy]carbonyl})amino)methyl]-3-methyl-1H-pyrrole-2-carboxylic acid
Methyl({2-[methyl(4-phenylbutyl)amino]-1-phenylethyl})amine
4,4-dimethyl-6-(propan-2-yl)-3,4-dihydro-2H-1-benzothiopyran-2-carboxylic acid
Methyl 2-amino-3-(4-chloro-3-fluorophenyl)-3-hydroxypropanoate
ethyl 5-amino-1-butyl-4-(propan-2-yl)-1H-pyrazole-3-carboxylate

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