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56856-83-8

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56856-83-8 Usage

Safety Profile

Suspected carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data. Poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Experimental teratogenic data. Human mutation data reported. When heated to decomposition it emits toxic fumes of NO,. See also NITROSAMINES, N-NITROSO COMPOUNDS, and ESTERS.

Check Digit Verification of cas no

The CAS Registry Mumber 56856-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56856-83:
(7*5)+(6*6)+(5*8)+(4*5)+(3*6)+(2*8)+(1*3)=168
168 % 10 = 8
So 56856-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H8N2O3/c1-4(7)9-3-6(2)5-8/h3H2,1-2H3

56856-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [methyl(nitroso)amino]methyl acetate

1.2 Other means of identification

Product number -
Other names N-Acetoxymethyl-N-nitrosomethylamin

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:56856-83-8 SDS

56856-83-8Relevant articles and documents

Synthesis of 14C labelled compounds. II. Synthesis of 14C methylacetoxy methylnitrosamine

Braun,Wiessler

, p. 379 - 383 (1977)

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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.

Oxidative decarboxylation of nitrosoamino acids: A synthetic approach to cyclic α-acetoxynitrosamines

Saavedra

, p. 1923 - 1926 (2007/10/05)

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