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N-Methyl-N-ethylacetamide, with the molecular formula C6H13NO, is a chemical compound derived from acetamide. It features N-ethyl and N-methyl groups attached to the nitrogen atom, giving it unique properties. This colorless liquid with a faint odor is relatively stable under normal conditions, but it requires careful handling due to its potential harmful effects if swallowed, inhaled, or causing skin and eye irritation.

38806-26-7

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38806-26-7 Usage

Uses

Used in Pharmaceutical Industry:
N-Methyl-N-ethylacetamide is utilized as a solvent in various chemical reactions, particularly in the pharmaceutical sector. Its properties make it suitable for facilitating reactions that are crucial for the synthesis of pharmaceutical compounds.
Used in Organic Compound Production:
Beyond its solvent role, N-Methyl-N-ethylacetamide also serves as a reactant in the production of other organic compounds. Its reactivity and stability contribute to the formation of desired products in organic synthesis processes.

Check Digit Verification of cas no

The CAS Registry Mumber 38806-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,0 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38806-26:
(7*3)+(6*8)+(5*8)+(4*0)+(3*6)+(2*2)+(1*6)=137
137 % 10 = 7
So 38806-26-7 is a valid CAS Registry Number.

38806-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-methylacetamide

1.2 Other means of identification

Product number -
Other names N-METHYL-N-ETHYLACETAMIDE

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:38806-26-7 SDS

38806-26-7Relevant academic research and scientific papers

N-Alkylation of N-trimethylsilyl derivatives of lactams, amides, and imides with alkyl sulfonates

Baukov, Yu. I.,Kramarova, E. P.,Negrebetsky, Vad. V.,Shagina, A. D.,Shipov, A. G.,Tarasenko, D. V.

, p. 398 - 400 (2020/04/15)

The reaction of N-trimethylsilyl derivatives of amides and imides with alkyl sulfonates on heating affords the corresponding N-alkyl derivatives and trimethylsilyl sulfonates.

PROCESS FOR PREPARING SECONDARY AMIDES BY CARBONYLATION OF A CORRESPONDING TERTIARY AMINE

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Page/Page column 4, (2010/06/14)

The present invention relates to a process for preparing secondary amides with good selectivity by carbonylating a corresponding tertiary amine with carbon monoxide in a reaction mixture in the presence of a metal catalyst and in the presence of a halogen containing promoter. The metal catalyst comprises palladium. A same or even a much better catalytic activity can be obtained with palladium than with the much more expensive rhodium, especially when the palladium is used in a low concentration. Moreover, also a good selectivity can be achieved.

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