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3-(ethoxycarbonyl)-1,1,1-triethyldiazathian-1-ium 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20133-49-7

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20133-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20133-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20133-49:
(7*2)+(6*0)+(5*1)+(4*3)+(3*3)+(2*4)+(1*9)=57
57 % 10 = 7
So 20133-49-7 is a valid CAS Registry Number.

20133-49-7SDS

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 ethoxycarbonylsulfamoyl(triethyl)azanium

1.2 Other means of identification

Product number -
Other names Triethylammonium-N-ethoxycarbonyl-sulfonamidat

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:20133-49-7 SDS

20133-49-7Relevant academic research and scientific papers

Crystal Structure of Burgess Inner Salts and their Hydrolyzed Ammonium Sulfaminates

Arduengo, Anthony J.,Uchiyama, Yosuke,DIxon, David A.,Vasiliu, Monica

, p. 867 - 873 (2019)

The solid-state structures of the Burgess reagent, and its analogous ethyl ester reveal structures indicative of triethylamine solvated sulfonyl imides rather than the more commonly depicted triethylammonium sulfonyl amidate. The existence of a reversibly formed hydrate of Burgess reagent is not supported by present studies, but rather a hydrosylate that does not revert to the Burgess reagent with gentle warming under vacuum was isolated and characterised. Structures of the hydrosylates from both the methyl- and ethyl-amidate esters were determined from X-ray crystallographic analysis and are reported. The crystal structures of the Burgess inner salts exhibit geometries at the sulfur atoms that are intermediate between a planar O2S=NCO2R unit and tetrahedral 4-coordinate sulfur centres that would be expected from a strong single (dative) bond between the triethylamine nitrogen and sulfur. The hydrolysed ammonium sulfaminates are water soluble intermolecular salts composed of triethylammonium ions, Et3NH+, and N-(alkoxycarbonyl)sulfaminate, O(-)SO2NHCO2R {R = CH3 or C2H5}.

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