256651-55-5

Basic information

• Product Name: Benzenemethanesulfonyl chloride, 2,6-dibromo-
• Synonyms: Benzenemethanesulfonyl chloride, 2,6-dibromo-;(2,6-DIBROMOPHENYL)METHANESULFONYL CHLORIDE
• CAS NO: 256651-55-5
• Molecular Formula: C₇H₅Br₂ClO₂S
• Molecular Weight: 348.4394
• Mol File: 256651-55-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 392.8±32.0 °C(Predicted)
• Appearance: /
• Density: 2.043±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenemethanesulfonyl chloride, 2,6-dibromo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanesulfonyl chloride, 2,6-dibromo-(256651-55-5)
• EPA Substance Registry System: Benzenemethanesulfonyl chloride, 2,6-dibromo-(256651-55-5)

Safety Data

• Hazardous Substances Data: 256651-55-5(Hazardous Substances Data)

Usage

Chemical Class

Sulfonyl chloride derivative

Main Properties

Strong electrophilic properties
Utilized as a reagent in organic synthesis
Used for introducing sulfonyl groups into organic molecules
Employed in pharmaceutical, agrochemical, and fine chemical production
Corrosive nature
Potential to cause skin and eye irritation

Specific Content

Molecular formula: C?H?Br?ClO?S
Electrophilic nature: Enables the introduction of sulfonyl groups into organic molecules
Application: Organic synthesis, pharmaceuticals, agrochemicals, and fine chemicals production
Safety considerations: Corrosive, can cause skin and eye irritation

Upstream product

• 108-36-1 1,3-dibromobenzene 
• 1013031-65-6 (2,6-dibromophenyl)methanol 
• 67713-23-9 2,6-dibromobenzaldehyde 
• 256651-54-4 C₉H₈Br₂OS 

Relevant articles and documents

Preparation process 2-6 - dibromobenzoyl chloride

The invention discloses a preparation process for 2,6-dibromobenzene methylsulfonyl chloride. The preparation process comprises the following steps: with m-dibromobenzene as a starting raw material, subjecting the m-dibromobenzene to a five-step reaction of acylation, reduction, chlorine substitution, substitution and sulfonyl chlorination so as to obtain a target compound namely the 2,6-dibromobenzene methylsulfonyl chloride. The process provided by the invention uses cheap and easily-available raw materials, has good safety by using NCS to replace chlorine gas as a chlorinating agent, and facilitates practical application.

INHIBITORS OF CYTOSOLIC PHOSPHOLIPASE A2

This invention provides chemical inhibitors of the activity of various phospholipase enzymes, particularly cytosolic phospholipase A2 enzymes (cPLA2), more particularly including inhibitors of cytosolic phospholipase A2 alpha enzymes (cPLAα). In some embodiments, the inhibitors have the Formula I: wherein the constituent variables are as defined herein.