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2-Nitroaminoethyl nitrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41719-24-8

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41719-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41719-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,1 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41719-24:
(7*4)+(6*1)+(5*7)+(4*1)+(3*9)+(2*2)+(1*4)=108
108 % 10 = 8
So 41719-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H5N3O5/c6-4(7)3-1-2-10-5(8)9/h3H,1-2H2

41719-24-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-NITROAMINOETHYL NITRATE

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:41719-24-8 SDS

41719-24-8Downstream Products

41719-24-8Relevant academic research and scientific papers

New synthetic approaches to functionally substituted 4,5-dihydro-1,2,3- oxadiazole 2-oxides

Tartakovskii,Ermakov,Strelenko,Vinogradov,Petrov

, p. 120 - 123 (2005)

A practical procedure has been proposed for the synthesis of functionally substituted 4,5-dihydro-1,2,3-oxadiazole 2-oxides on the basis ofsulfamic acid derivatives. 2005 Pleiades Publishing, Inc.

SYNTHESIS OF N-ACETOXYMETHYLNITROAMINE DERIVATIVES AND INVESTIGATION OF THEIR REACTIONS

Marchenko, G.A.,Punegova, L.N.,Shitova, T.S.,Roman'ko, N.A.,Egorova, L.S.,Kargin, Yu.M.

, p. 33 - 37 (2007/10/02)

A series of α,β'-substituted dialkylnitroamines were synthesized from N-2-nitrooxyethyl derivatives of N-acetoxymethylnitroamines by nucleophilic substitution reactions.The reactivity of N-chloroethyl-, N-nitroxyethyl-, and N-azidoethyl-N-acetoxymethylnitroamines in methylenebisnitroamine condensation reactions was studied.It was established that only N-chloroethyl-N-acetoxymethylnitroamines react with sulfuric acid to form N,N-chloroehtylenedinitroamines, the structure of which depends on the reaction conditions.On the basis of IR spectroscopic data it was shown that the integral intensity of the absorption bands for the antisymmetric stretching vibrations of the nitroamine group can be used for structure-group analysis of the nitroamines.

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