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CAS

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2905-29-5

2,6-Dimethylbenzenesulfonyl chloride, also known as 2,6-dimethyltoluene sulfonyl chloride or 2,6-dimethylbenzenesulfonyl chloride, is an organic compound with the chemical formula C8H9ClO2S. It is a colorless to pale yellow liquid with a pungent odor and is soluble in organic solvents. 2,6-DIMETHYLBENZENESULFONYL CHLORIDE is primarily used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and other sulfur-containing compounds. It is also employed as an intermediate in the production of pharmaceuticals, agrochemicals, and dyes. Due to its reactivity, it is essential to handle 2,6-dimethylbenzenesulfonyl chloride with care, as it can cause irritation to the skin, eyes, and respiratory system.

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  • 2905-29-5 Structure

  • Basic information

    1. Product Name: 2,6-DIMETHYLBENZENESULFONYL CHLORIDE
    2. Synonyms: 2,6-DIMETHYLBENZENESULFONYL CHLORIDE;BUTTPARK 121\11-85;2,6-DIMETHYLBENZENE-1-SULFONYL CHLORIDE;2,6-Xylenesulfonyl Chloride
    3. CAS NO:2905-29-5
    4. Molecular Formula: C8H9ClO2S
    5. Molecular Weight: 204.67
    6. EINECS: N/A
    7. Product Categories: Aromatics;Sulfur & Selenium Compounds
    8. Mol File: 2905-29-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 291.3 °C at 760 mmHg
    3. Flash Point: 130 °C
    4. Appearance: /
    5. Density: 1.29 g/cm3
    6. Vapor Pressure: 0.00344mmHg at 25°C
    7. Refractive Index: 1.538
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,6-DIMETHYLBENZENESULFONYL CHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,6-DIMETHYLBENZENESULFONYL CHLORIDE(2905-29-5)
    12. EPA Substance Registry System: 2,6-DIMETHYLBENZENESULFONYL CHLORIDE(2905-29-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2905-29-5(Hazardous Substances Data)

2905-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2905-29-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2905-29:
(6*2)+(5*9)+(4*0)+(3*5)+(2*2)+(1*9)=85
85 % 10 = 5
So 2905-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClO2S/c1-6-4-3-5-7(2)8(6)12(9,10)11/h3-5H,1-2H3

2905-29-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dimethylbenzenesulfonyl Chloride

1.2 Other means of identification

Product number -
Other names 2,6-dimethylphenylsulfonyl chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2905-29-5 SDS

2905-29-5Relevant articles and documents

Inhibitors of cytosolic phospholipase A2

-

, (2008/06/13)

This invention provides substituted indole compounds of the general formula: and pharmaceutically acceptable salt forms thereof, and methods for using the compounds as inhibitors of the activity of various phospholipase enzymes, particularly phospholipase A2 enzymes, and for the medical treatment, prevention and inhibition of pain and inflammation.

Conversion of sterically hindered phenols into the corresponding N,N-dimethylarenesulfonamides via the Newman-Kwart rearrangement

Wagenaar, Anno,Engberts, Jan B. F. N.

, p. 91 - 94 (2007/10/02)

The 2-alkyl- and 2,6-dialkylbenzenesulfonyl chlorides 5a-f were obtained in high yield by chlorination of the correspondingly substituted S-aryl N,N-dialkylthiocarbamates 4a-g.These precursors have been synthesized via the Newman-Kwart rearrangement of th

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