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Carbamic acid, [[(4-methylphenyl)sulfonyl]methyl]nitroso-, ethyl ester, is a complex organic compound with the chemical formula C11H14N2O5S. It is an ester derivative of carbamic acid, featuring a nitroso group and a sulfonyl group attached to a methylphenyl ring. Carbamic acid, [[(4-methylphenyl)sulfonyl]methyl]nitroso-, ethyl ester is characterized by its potential reactivity and may be used in the synthesis of various pharmaceuticals and chemical intermediates. Due to its specific structure, it is important to handle Carbamic acid, [[(4-methylphenyl)sulfonyl]methyl]nitroso-, ethyl ester with care, as it may have specific safety and stability considerations.

2951-53-3

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2951-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2951-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2951-53:
(6*2)+(5*9)+(4*5)+(3*1)+(2*5)+(1*3)=93
93 % 10 = 3
So 2951-53-3 is a valid CAS Registry Number.

2951-53-3SDS

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 ethyl N-[(4-methylphenyl)sulfonylmethyl]-N-nitrosocarbamate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:2951-53-3 SDS

2951-53-3Relevant academic research and scientific papers

Theory-guided discovery of unique chemical transformations of cyclopropenes

Weatherhead-Kloster, Robin A.,Corey

, p. 171 - 174 (2007/10/03)

(Chemical Equation Presented) Chiral 2-cyclopropenyl-4-tolyl sulfones, available by the [2 + 1]-cycloaddition of tosyldiazomethane to acetylenes under catalysis by the Rh(II) complex 1, provide a number of unusual transformations and useful chiral product

Improved preparation of tosyldiazomethane

Plessis,Uguen,De Cian,Fischer

, p. 5489 - 5493 (2007/10/03)

Treatment of the carbamate 2a by i-amyl nitrite and TMSCl in presence of a reduced amount of pyridine, followed by decomposition of the resulting nitroso derivative 3a with activated alumina afforded in high yield the pure, crystalline, diazosulfone 1a, a

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