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Benzamide, 2,3-dimethoxy-N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74826-20-3

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74826-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74826-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,2 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74826-20:
(7*7)+(6*4)+(5*8)+(4*2)+(3*6)+(2*2)+(1*0)=143
143 % 10 = 3
So 74826-20-3 is a valid CAS Registry Number.

74826-20-3SDS

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 2,3-dimethoxy-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names N-methyl-2,3-dimethoxybenzamide

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:74826-20-3 SDS

74826-20-3Relevant academic research and scientific papers

Synthesis of some mellein derivatives

Bhide, B H,Akolkar, V D,Brahmbhatt, D I

, p. 116 - 117 (2007/10/02)

Synthesis of some mellein derivatives (IIIa-d) have been carried out using o-lithiation reaction. o-Lithiation of substituted N-methylbenzamides (Ia-d) and with n-BuLi followed by alkylation with propylene oxide gives 3-methyl-3,4-dihydroisocoumarins (IIa-c) and 5,6-dimethoxymellein (IIId). (IIa-c) have been converted to IIIa-c by HBr/AcOH or anhyd.AlCl3.

A NEW PATHWAY TO 1,3,4(2H)-ISOQUINOLINETRIONES AND SUBSTITUTED ISOINDOLINONES

Vekemans, Jozef,Hoornaert, Georges

, p. 943 - 950 (2007/10/02)

A new synthesis in the isoquinoline series is discussed: the reaction of appropriate benzamides and oxalyl chloride affords isoquinolinetrions along N-aroyloxamoyl chlorides.The solvent effect, the acid catalysis and the isomer distribution are accounted

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