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N-nitroso(acetoxybenzyl)methylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53198-46-2

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53198-46-2 Usage

Safety Profile

Mutation data reported. Many Nnitroso compounds are carcinogens. When heated todecomposition it emits toxic fumes of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 53198-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53198-46:
(7*5)+(6*3)+(5*1)+(4*9)+(3*8)+(2*4)+(1*6)=132
132 % 10 = 2
So 53198-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O3/c1-8(13)15-10(12(2)11-14)9-6-4-3-5-7-9/h3-7,10H,1-2H3

53198-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(α-Acetoxybenzyl)-N-nitrosomethylamin

1.2 Other means of identification

Product number -
Other names Methyl(α-acetoxybenzyl)nitrosamin

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:53198-46-2 SDS

53198-46-2Downstream Products

53198-46-2Relevant academic research and scientific papers

The Chemistry of Nitrosamines, IV. - Syntheses of α-C-Functionalized N-Nitrosodialkylamines: Esters and Ethers of 1-alcohols

Mueller, Eduard,Kettler, Regina,Wiessler, Manfred

, p. 1468 - 1493 (2007/10/02)

Imines (Schiff's bases) and nitrosyl chloride react to give N-alkyl-1-chloro-N-nitrosoalkylamines 13.Nucleophilic substitution by acetate or p-nitrobenzoate affords the acetates 7 and 9 and p-nitrobenzoates 8 and 10, respectively.The spectroscopic and chemical data of the newly synthesized compounds are discussed.

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