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Home > Encyclopedia > 4-Chlorobenzenesulfonyl chloride

4-Chlorobenzenesulfonyl chloride

4-Chlorobenzenesulfonyl chloride structure

4-Chlorobenzenesulfonyl chloride 

structure
  • CAS No:

    98-60-2

  • Formula:

    C6H4Cl2O2S

  • Chemical Name:

    4-Chlorobenzenesulfonyl chloride

  • Synonyms:

    Benzenesulfonyl chloride,4-chloro-;Benzenesulfonyl chloride,p-chloro-;4-Chlorobenzenesulfonyl chloride;p-Chlorobenzenesulfonyl chloride;p-Chlorophenylsulfonyl chloride;4-Chlorophenylsulfonyl chloride;NSC 6956;4-Chlorobenzene-1-sulfonyl chloride;27415-01-6

  • Categories:

    Organic Chemistry  >  Hydrocarbons and Derivatives

Description

white to light yellow crystals, powder or flakes

4-Chlorobenzenesulfonyl chloride Basic Attributes

211.07

211.07

511583

202-685-3

H55O3362D6

6956

DTXSID4059174

PRISMS OR PLATES FROM ETHER

29049020

Characteristics

42.5

1.8

Clear Liquid

1.5±0.1 g/cm3

55 °C

141 °C @ Press: 15 Torr

226 °F

1.569

H2O: INsoluble ;VERY SOL IN ETHER & BENZENE

Oral-rat LD50: 4250 mg/kg; Abdominal cavity-mouse LDL0:250 mg/kg

Thermal decomposition to emit toxic sulfur oxide fumes

DECOMP IN HOT WATER & HOT ALCOHOL

Safety Information

II

8

UN 3261 8/PG 2

2

34-37

26-28-36/37/39-45

DB8925000

C

The warehouse is low-temperature, ventilated and dry

Corrosive

P280-P305 + P351 + P338-P310

H314

UN 3261 8/PG 2

P280; P305 + P351 + P338; P310

|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 90 companies from 5 notifications to the ECHA C&L Inventory.

Toxicity

moderately toxic

4-Chlorobenzenesulfonyl chloride Use and Manufacturing

Methods of Manufacturing

The preparation method is prepared by chlorobenzene sulfonation. Mix chlorosulfonic acid and fuming sulfuric acid and cool to below 20℃, add chlorobenzene under vigorous stirring, react at 23~25℃ for 2~3 h, then heat up at 60℃ for 2 h, cool, filter and wash off It is acidic. In addition, it can also be obtained by reacting p-chlorobenzenesulfonic acid with chlorosulfonic acid at 60°C for 1.5 h.

Uses

This product is mainly used in the preparation of medicine, engineering plastics, pesticide intermediates and organic synthetic raw material p-chlorobenzenesulfonamide. Used in the production of pesticide acaricide mite egg ester, medical Telden, etc.

Benzenesulfonyl chloride, 4-chloro-: ACTIVE

Computed Properties

Molecular Weight:211.06
XLogP3:1.8
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:209.9309059
Monoisotopic Mass:209.9309059
Topological Polar Surface Area:42.5
Heavy Atom Count:11
Complexity:211
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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