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Benzoyl chloride, 2,3-dimethoxy-4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77869-41-1

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77869-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77869-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,6 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77869-41:
(7*7)+(6*7)+(5*8)+(4*6)+(3*9)+(2*4)+(1*1)=191
191 % 10 = 1
So 77869-41-1 is a valid CAS Registry Number.

77869-41-1SDS

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 2,3-dimethoxy-4-methylbenzoyl chloride

1.2 Other means of identification

Product number -
Other names 2,3-Dimethoxy-4-methyl-benzoylchlorid

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:77869-41-1 SDS

77869-41-1Relevant academic research and scientific papers

Synthesis of the Bacterial Coenzyme Methoxatin

Gainor, James A.,Weinreb, Steven M.

, p. 2833 - 2837 (2007/10/02)

The details of a total synthesis of methoxatin (1), the coenzyme of several bacterial alcohol dehydrogenases, are presented.Methoxatin has been prepared in 13 steps by starting from 2,3-dimethoxytoluene.The successful synthetic strategy for construction of the coenzyme used a Pfitzinger synthesis for preparation of the quinoline dicarboxylic acid portion of 1 and an "umpolung" variation of the Reissert indole synthesis for annulation of the remaining pyrrole ring.

Preparation and Catalytic Hydrogenation of 4,6-Dimethyl- and 4,7-Dimethyl-8-methoxycoumarins. A 4-Methyldihydrocoumarin Synthesis

Mills, Frank D.

, p. 1597 - 1600 (2007/10/02)

Reduction of the title coumarins at 1500 psi and 150 deg over 10percent palladium on charcoal provides a simple route to dihydrocoumarins and/or ethylbutanoates, hydrogenolysis products of the lactone.Lower pressures and temperatures tend to yield only th

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