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Benzoic acid, 2-[(1-carboxy-2,5-dimethoxy-2,5-cyclohexadien-1-yl)methyl]-6-methoxy-, 1-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73177-43-2

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73177-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73177-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,7 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73177-43:
(7*7)+(6*3)+(5*1)+(4*7)+(3*7)+(2*4)+(1*3)=132
132 % 10 = 2
So 73177-43-2 is a valid CAS Registry Number.

73177-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dimethoxy-1-<(3'-methoxy-2'-(methoxycarbonyl)phenyl)methyl>-2,5-cyclohexadiene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,5-dimethoxy-1-(3'-methoxy-2'-methoxycarbonylphenyl)methylcyclohexa-2,5-diene-1-carboxylic acid

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:73177-43-2 SDS

73177-43-2Relevant academic research and scientific papers

Studies on Gibberellin Synthesis: The Total Synthesis of Gibberellic Acid from Hydrofluorenone Intermediates

Hook, James M.,Mander, Lewis N.,Urech, Rudolf

, p. 3250 - 3260 (2007/10/02)

Reductive alkylation of 2,5-dimethoxybenzoic acid with benzyl iodide 15 followed by cyclodehydration furnished fluorenone 8 which was converted into gibbane 10 by means of an acid-catalyzed intramolecular cyclization procedure based on diazo ketone 21.Ben

Studies on Reductive Alkylation. Regiocontrolled Synthesis of Anthracene Derivatives

Mander, Lewis N.,Woolias, Michael

, p. 2249 - 2252 (2007/10/02)

Reductive alkylation of 2,5-dimethoxybenzoic acid, its 4-methyl derivative, and 3,5-dimethoxybenzoic acid with methyl 2-iodomethyl-6-methoxybenzoate furnished acids (1), (2) and (3), respectively.Oxidative decarboxylation followed by hydrolysis led to dip

Reductive Alkylation of 2,5-Dimethoxybenzoic Acid: A Direct Synthesis of Dihydrofluoren-2-ones

Hook, James M.,Mander, Lewis N.

, p. 1722 - 1724 (2007/10/02)

A two-operation procedure is described for the synthesis of 3,4-dihydrofluoren-2(1H)-ones from "reductive alkylation" of 2,5-dimethoxybenzoic acid with benzyl halides, followed by cyclodehydration of the adducts, with concomitant decarboxylation.

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