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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Sulfonyl halide >2-(METHYLSULFONYL)BENZENESULFONYL CHLORIDE

2-(METHYLSULFONYL)BENZENESULFONYL CHLORIDE

2-(METHYLSULFONYL)BENZENESULFONYL CHLORIDE Structure
  • ₹0
  • Product name: 2-(METHYLSULFONYL)BENZENESULFONYL CHLORIDE
  • CAS: 89265-35-0
  • MF: C7H7ClO4S2
  • MW: 254.71
  • EINECS:
  • MDL Number:MFCD00216493
  • Synonyms:o-Chlorosulfonylphenyl methyl sulfone.;2-Methysulfonylbenzenesulfonyl chloride;2-(Methylsulfonyl)benzenesulfonyl chloride,95%;2-(Methylsulphonyl)benzenesulphonyl chloride 95%;2-(Chlorosulphonyl)phenyl methyl sulphone;2-(METHYLSULFONYL)BENZENESULFONYL CHLORIDE;2-METHYLSULPHONYLBENZENESULFONYL CHLORIDE;2-METHYLSULPHONYLBENZENESULPHONYL CHLORIDE
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :133-138 °C
Boiling point :442.0±37.0 °C(Predicted)
Density :1.4936 (estimate)
form :Crystalline Powder
color :Off-white to yellow-brown
Water Solubility :Reacts with water.
Sensitive :Moisture Sensitive
CAS DataBase Reference :89265-35-0(CAS DataBase Reference)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H314 Causes severe skin burns and eye damage Skin corrosion/irritation Category 1A, B, C Danger GHS hazard pictograms P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
H318 Causes serious eye damage Serious eye damage/eye irritation Category 1 Danger GHS hazard pictograms P280, P305+P351+P338, P310
Precautionary statements:
P301+P330+P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P303+P361+P353 IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405 Store locked up.

Description

It finds its application in the synthesis and biological evaluation of inhibitors of thymidine monophosphate kinase from bacillus anthracis.

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