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67557-57-7

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67557-57-7 Usage

General Description

[(2H3)methyl(nitroso)amino]methyl acetate is a chemical compound with the molecular formula C4H7NO4 and a molecular weight of 133.10 g/mol. It is a derivative of acetate, containing a methyl group, a nitroso functional group, and an amino group. The compound is a synthetic intermediate used in organic chemical reactions and research. It is commonly used in the production of pharmaceuticals and agrochemicals, as well as in the synthesis of other complex organic compounds. The compound's specific properties, such as its reactivity and potential hazards, would depend on the context of its use and its concentration.

Check Digit Verification of cas no

The CAS Registry Mumber 67557-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,5 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67557-57:
(7*6)+(6*7)+(5*5)+(4*5)+(3*7)+(2*5)+(1*7)=167
167 % 10 = 7
So 67557-57-7 is a valid CAS Registry Number.

67557-57-7SDS

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 [nitroso(trideuteriomethyl)amino]methyl acetate

1.2 Other means of identification

Product number -
Other names Acetoxymethyltrideuteromethylnitrosamine

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:67557-57-7 SDS

67557-57-7Downstream Products

67557-57-7Relevant articles and documents

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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