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1,3-Benzodioxole-5-carboxylic acid, 6-(6-formyl-2,3,4-trimethoxyphenyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65171-01-9

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65171-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65171-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,7 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65171-01:
(7*6)+(6*5)+(5*1)+(4*7)+(3*1)+(2*0)+(1*1)=109
109 % 10 = 9
So 65171-01-9 is a valid CAS Registry Number.

65171-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name formyl-2 methoxycarbonyl-2' methylenedioxy-4',5' trimethoxy-4,5,6 biphenyle

1.2 Other means of identification

Product number -
Other names 6-(6-formyl-2,3,4-trimethoxyphenyl)benzo[d][1,3]dioxole-5-carbaldehyde

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:65171-01-9 SDS

65171-01-9Relevant academic research and scientific papers

CHEMICAL COMPOUNDS

-

Page/Page column 68, (2008/12/06)

A compound of formula (I) is described; wherein the substituents are as defined in the text and wherein the compound is intended for use in the production of a vascular damaging effect in a warm-blooded animal.

SYNTHESES TOTALES ET ETUDES DE LIGNANES BIOLOGIQUEMENT ACTIFS-I. APPLICATION DE LA REACTION D'ULLMANN A LA SYNTHESE DE BIARYLES PRECURSEURS DE LIGNANES BISBENZOCYCLOOCTADIENES

Brown, Eric,Robin, Jean-Pierre,Dhal, Robert

, p. 2569 - 2580 (2007/10/02)

Several biaryls bearing various substituents on both rings were synthesized in a preparativ fashion, and in yields up to 88percent by a technical improvement on the classical Ullmann reaction.All these biaryls bear reactive functional groups (i.e. formyl, methoxycarbonyl, dimethoxycarbonylpropyl and butanolidylmethyl) in both the o and o' positions.The biaryls 9, 13, 21 and 26-33 are plausible synthons for bisbenzocyclooctadiene lignans such as schizandrin and steganacin.

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