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

54818-95-0

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54818-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54818-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54818-95:
(7*5)+(6*4)+(5*8)+(4*1)+(3*8)+(2*9)+(1*5)=150
150 % 10 = 0
So 54818-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO/c1-5-14(6-2)13(15)12-8-7-10(3)9-11(12)4/h7-9H,5-6H2,1-4H3

54818-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-2,4-dimethylbenzamide

1.2 Other means of identification

Product number -
Other names BENZAMIDE,N,N-DIETHYL-2,4-DIMETHYL

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:54818-95-0 SDS

54818-95-0Relevant academic research and scientific papers

Synthesis of 12-oxobenzo[c]phenanthridinones and 4-substituted 3-arylisoquinolones via Vilsmeier-Haack reaction

Khadka, Daulat Bikram,Yang, Su Hui,Cho, Suk Hee,Zhao, Chao,Cho, Won-Jea

, p. 250 - 261 (2012/01/05)

Vilsmeier-Haack reaction on 3-arylisoquinolones resulted in versatile 4-formylated 3-arylisoquinolones that were further derivatized into 12-oxobenzo[c]phenanthridinones, 4-alkoxymethyl-3-arylisoquinolones, 3-aryl-4-phenoxymethylisoquinolones, 4-aminometh

Total synthesis of 8-oxypseudopalmatine and 8-oxypseudoberberine via ring-closing metathesis

Van, Hue Thi My,Yang, Su Hui,Khadka, Daulat Bikram,Kim, Yong-Chul,Cho, Won-Jea

experimental part, p. 10142 - 10148 (2010/02/27)

Concise synthesis of 8-oxypseudopalmatine and 8-oxypseudoberberine has been achieved using ruthenium-catalyzed ring-closing metathesis (RCM) as the key step, in which the RCM substrates, 3-arylisoquinolinones, were prepared by lithiated cycloaddition reac

BISCARBAMOYL DISELENIDES AS NEW CARBAMOYLATING REAGENTS. LEWIS ACID PROMOTED CARBAMOYLATION OF AROMATIC COMPOUNDS

Fujiwara, Shin-Ichi,Ogawa, Akiya,Kambe, Nobuaki,Ryu, Ilhyong,Sonoda, Noboru

, p. 6121 - 6124 (2007/10/02)

The reaction of biscarbamoyl diselenides with aromatic compounds in the presence of Lewis acids resulted in Friedel-Crafts type carbamoylation (Gatterman amide synthesis) to give corresponding aromatic amides in good yields.This methodology was successfully applied to aroylation and benzylation by use of dibenzoyl diselenide and dibenzyl diselenide, respectively.

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