3-Chloro-4-methylbenzenesulfonyl chloride

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Names

[ CAS No. ]:
42413-03-6

[ Name ]:
3-Chloro-4-methylbenzenesulfonyl chloride

[Synonym ]:
Benzenesulfonyl chloride, 3-chloro-4-methyl-
MFCD00203987
3-CHLORO-4-METHYLBENZENE-1-SULFONYL CHLORIDE
3-Chloro-4-methylbenzenesulfonyl chloride
EINECS 412-890-1

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
305.7±35.0 °C at 760 mmHg

[ Melting Point ]:
34-38 °C(lit.)

[ Molecular Formula ]:
C7H6Cl2O2S

[ Molecular Weight ]:
225.092

[ Flash Point ]:
138.7±25.9 °C

[ Exact Mass ]:
223.946548

[ PSA ]:
42.52000

[ LogP ]:
3.41

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.559

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H317-H412

[ Precautionary Statements ]:
P273-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C:Corrosive;

[ Risk Phrases ]:
R34;R43;R52/53

[ Safety Phrases ]:
S23-S26-S36/37/39-S45-S61

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
2

[ Packaging Group ]:
II

[ Hazard Class ]:
8

[ HS Code ]:
2904909090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Tosyl chloride
  • 2-chlorotoluene-4-sulphonic acid

DownStream

  • 2-Chlorotoluene
  • Benzenesulfonamide, 3-chloro-4-methyl-
  • 2,4-Dichlorobenzotrichloride
  • Benzenesulfonic acid,5-chloro-4-methyl-2-nitro-
  • Benzene,1,2,3,4,5-pentachloro-6-methyl-
  • 3-Chloro-4-methyl-5-nitrobenzenesulfonyl chloride
  • 2-chlorotoluene-4-sulphonic acid

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

Design and synthesis of substituted nicotinamides as inhibitors of soluble epoxide hydrolase

Bioorg. Med. Chem. Lett. 19(20) , 5864-5868, (2009)

A series of potent nicotinamide inhibitors of soluble epoxides hydrolase (sEH) is disclosed. This series was designed using structure-based deconstruction and a combination of two HTS hit series, resu...

Wiley-VCH

Ullmann's Fine Chemicals , (2014), 295


More Articles

Related Compounds

  • 3-Chloro-4-fluorobenzoyl chloride
  • 3-Chloro-4-isopropoxybenzoyl chloride
  • 3-Chloro-4-methylbenzoyl chloride
  • 3-Chloro-4-fluorobenzenesulfonyl chloride
  • 3-CHLORO-4-METHOXYBENZYL CHLORIDE
  • 3-Chloro-4-isopropoxybenzenesulfonyl chloride
  • 2-(4-methylpyridin-3-yl)-3,4-dihydro-2,7-naphthyridin-1(2H)-one
  • 3-(3,5-Difluorophenoxy)pyrrolidine
  • N-cyclobutyl-2-methylpyrimidin-4-amine
  • 1-(3,4-Dihydroxyphenyl)-2-(methylsulfonyl)ethanone
  • 3-amino-5H,7H,8H-6lambda6-thiopyrano[4,3-c]pyridazine-6,6-dione
  • 5H,7H,8H-thiopyrano[4,3-c]pyridazin-3-amine
  • 1-(Azetidin-3-yl)-4-isopropylpiperazine
  • tert-butyl N-[1-hydroxy-3-(pyridin-3-yl)propan-2-yl]carbamate
  • 3-[(2-Ethylcyclohexyl)oxy]azetidine
  • 3-(1-Phenylethoxy)azetidine
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