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Methanesulfonamide, N-(methylsulfonyl)-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64183-75-1

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64183-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64183-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,8 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64183-75:
(7*6)+(6*4)+(5*1)+(4*8)+(3*3)+(2*7)+(1*5)=131
131 % 10 = 1
So 64183-75-1 is a valid CAS Registry Number.

64183-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-methylsulfonylmethanesulfonamide

1.2 Other means of identification

Product number -
Other names N-Benzyldimesylamin

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:64183-75-1 SDS

64183-75-1Downstream Products

64183-75-1Relevant academic research and scientific papers

Synthesis and reactivity of polydisulfonimides

Burlingham,Widlanski

, p. 2937 - 2945 (2007/10/03)

The first synthesis of alkyl disulfonimide oligomers is presented. In the process of synthesizing these oligomers, previously unreported reactivity of the N-substituted disulfonimide functional group was discovered. Under basic conditions, unexpected lengthening of the oligomers occurs through a "transdisulfonimidation" reaction, whereby new disulfonimides are synthesized from existing ones by reaction with sulfonamide anion. This process appears to proceed via formation of a sulfene intermediate. Support for the E1cBRev mechanism includes isotope scrambling, substituent effects, and sulfene trapping.

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