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N,N-Diethyl-2,4,6-trimethylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34274-11-8

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34274-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34274-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,7 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34274-11:
(7*3)+(6*4)+(5*2)+(4*7)+(3*4)+(2*1)+(1*1)=98
98 % 10 = 8
So 34274-11-8 is a valid CAS Registry Number.

34274-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-2,4,6-trimethylbenzamide

1.2 Other means of identification

Product number -
Other names -

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:34274-11-8 SDS

34274-11-8Downstream Products

34274-11-8Relevant academic research and scientific papers

Direct Synthesis of Enamides via Electrophilic Activation of Amides

Berger, Martin,Kaiser, Daniel,Maulide, Nuno,Spie?, Philipp

supporting information, p. 10524 - 10529 (2021/07/28)

A novel, one-step N-dehydrogenation of amides to enamides is reported. This reaction employs the unlikely combination of LiHMDS and triflic anhydride, which serves as both the electrophilic activator and the oxidant, and is characterized by its simple setup and broad substrate scope. The synthetic utility of the formed enamides was readily demonstrated in a range of downstream transformations.

Asymmetric synthesis of enantiomerically enriched atropisomeric amides by desymmetrisation of N,N-dialkylmesitamides

Clayden, Jonathan,Johnson, Paul,Pink, Jennifer H.

, p. 371 - 375 (2007/10/03)

Asymmetric synthesis of enantiomerically enriched atropisomeric amides was carried out by desymmetrisation of N,N-dialkylmesitamides. Lithiation and silylation of the latter using chiral lithium amide bases was performed. The technique of including an ele

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