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N-NITROSO-O,N-DIETHYL-HYDROXYLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56235-95-1

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56235-95-1 Usage

Safety Profile

Moderately toxic by ingestion.When heated to decomposition it emits toxic fumes ofNOx. See also N-NITROSO COMPOUNDS andAMINES

Check Digit Verification of cas no

The CAS Registry Mumber 56235-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,3 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56235-95:
(7*5)+(6*6)+(5*2)+(4*3)+(3*5)+(2*9)+(1*5)=131
131 % 10 = 1
So 56235-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2O2/c1-3-6(5-7)8-4-2/h3-4H2,1-2H3

56235-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-5-nitro-N-[[4-(trifluoromethyl)phenyl]methyl]aniline

1.2 Other means of identification

Product number -
Other names N-nitroso-O,N-diethyl hydroxylamine

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:56235-95-1 SDS

56235-95-1Relevant academic research and scientific papers

THE FORMATION OF AZOXYALKANES IN REACTIONS OF SOME ORGANOMETALLIC REAGENTS WITH N-nitroso-O,N-DIALKYLHYDROXYLAMINES: THE NONPHOTOCHEMICAL SYNTHESIS OF AN ACYCLIC (E)-AZOXYALKANE

Meesters, A. C. M.,Rueerger, H.,Rajeswari, K.,Benn, M. H.

, p. 264 - 268 (2007/10/02)

Azoxyalkanes were found to be regiospecifically formed in the reactions of some alkyllithium and Grignard reagents with N-nitroso-O,N-dialkylhydroxylamines.Remarkably, although (Z)-stereomers were usually produced, in one case the (E)-isomer was predominant.

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