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
4-(4-cyano-5-((pyridin-3-ylmethyl)amino)oxazol-2-yl)-N,N-dimethylbenzenesulfonamide
3-[1-(Hydroxyimino)ethyl]-2,2-dimethylcyclobutane-1-carboxylic acid
6-chloro-3,4-dihydro-2H-chromen-8-ylamine
4-(5-(azepan-1-yl)-4-cyanooxazol-2-yl)-N,N-diethylbenzenesulfonamide
(2R,3R)-(3-Hydroxymethyl-1,4-dioxa-spiro[4.4]non-2-yl)-methanol
N1-(4-(azepan-1-yl)pyrimidin-2-yl)ethane-1,2-diamine
5-(4-Methylpiperidin-1-yl)-2-(4-(piperidin-1-ylsulfonyl)phenyl)oxazole-4-carbonitrile
8H-Acenaphtho[1,2-c]pyrrole
5-[(2-Chlorobenzyl)amino]-2-[4-(piperidin-1-ylsulfonyl)phenyl]-1,3-oxazole-4-carbonitrile
Tetrahydro-2-[(phenylmethyl)thio]furan

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