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Sulfamoyl chloride, (triphenylphosphoranylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41309-06-2

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41309-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41309-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,0 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41309-06:
(7*4)+(6*1)+(5*3)+(4*0)+(3*9)+(2*0)+(1*6)=82
82 % 10 = 2
So 41309-06-2 is a valid CAS Registry Number.

41309-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(triphenyl-λ<sup>5</sup>-phosphanylidene)sulfamoyl chloride

1.2 Other means of identification

Product number -
Other names chlorosulfonylimino(triphenyl)phosphorane

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:41309-06-2 SDS

41309-06-2Upstream product

41309-06-2Downstream Products

41309-06-2Relevant academic research and scientific papers

Chemistry of (triphenylphosphoranylidene)sulfamoyl chloride. I. Reaction with amines and alcohols

Arrington, Dale E.

, p. 1236 - 1238 (2007/10/16)

Compounds of the type Ph3PNSO2OR and Ph3PNSO2NHR (R = Me, Et, n-Pr, n-Bu, and o-, m-, p-BrC6H4) have been prepared in good yield by the reaction of (triphenylphosphoranylidene)sulfamoyl chloride, Ph3PNSO2Cl, with alcohols in pyridine or with amines in chloroform; derivatives of secondary amines may also be prepared by the latter method. Heating the methyl ester in pyridine to moderately high temperatures produces a compound containing the Ph3PNSO2O- ion which yields the free acid upon acidification. The infrared spectra of the title compound and the alkyl esters in the 1100-1300-cm-1 region are presented and discussed.

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