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3,5-Dimethoxy-1,2-benzenedicarboxylic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24953-73-9

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24953-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24953-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24953-73:
(7*2)+(6*4)+(5*9)+(4*5)+(3*3)+(2*7)+(1*3)=129
129 % 10 = 9
So 24953-73-9 is a valid CAS Registry Number.

24953-73-9SDS

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 dimethyl 3,5-dimethoxybenzene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3,5-dimethoxy-phthalic acid dimethyl ester

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:24953-73-9 SDS

24953-73-9Relevant articles and documents

Diels-Alder reaction of methoxythiophenes: A new one-pot synthesis of dimethyl phthalates

Corral,Lissavetzky,Manzanares

, p. 29 - 31 (2007/10/03)

A series of dimethyl phthalates have been prepared from methoxythiophenes and dimethyl acetylenedicarboxylate (DMAD) in xylene. When the reaction is carried out in acetic acid, thienylfumarates are obtained.

Evaluation of some preparations of trialkoxyphthalic acid derivatives

Parker, Kathlyn A.,Spero, Denice M.,Koziski, Kathleen A.

, p. 183 - 188 (2007/10/02)

Several approaches to trialkoxyphthalic acid derivatives, potential intermediates in a fredericamycin synthesis, were tested. Sequences based on a Diels-Alder/retro Diels-Alder reaction, a cyanide addition to a quinone, an Elbe oxidation, and an amide-directed ortho-lithiation are discussed in terms of length, yields, convenience, and the versatility of the product of each.

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