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61738-05-4

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61738-05-4 Usage

Safety Profile

Poison by ingestion. Questionable carcinogen with experimental carcinogenic data. When heated to decomposition it emits toxic fumes of NOx. See also NITROSAMINES.

Check Digit Verification of cas no

The CAS Registry Mumber 61738-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,3 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61738-05:
(7*6)+(6*1)+(5*7)+(4*3)+(3*8)+(2*0)+(1*5)=124
124 % 10 = 4
So 61738-05-4 is a valid CAS Registry Number.

61738-05-4SDS

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 N-(1-methoxyethyl)-N-methylnitrous amide

1.2 Other means of identification

Product number -
Other names 1-Methoxy-aethyl-methylnitrosamin

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:61738-05-4 SDS

61738-05-4Relevant 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.

N-Nitrosoenamines, Versatile New Synthesis Intermediates

Kupper, Robert,Michejda, Christopher J.

, p. 2919 - 2921 (2007/10/02)

N-Nitrosoenamines are reactive toward nucleophilic reagents such as dialkylcopper lithium and enolate ions, as well as being active in electrophilic reactions such as acid-catalyzed additions.

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