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2,3-Naphthalenedicarboxylic acid, 4-(3,4-dimethoxyphenyl)-1-hydroxy-5,6,7-trimethoxy-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104756-80-1

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104756-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104756-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,5 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104756-80:
(8*1)+(7*0)+(6*4)+(5*7)+(4*5)+(3*6)+(2*8)+(1*0)=121
121 % 10 = 1
So 104756-80-1 is a valid CAS Registry Number.

104756-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,4-dimethoxyphenyl)-2,3-bis(ethoxycarbonyl)-4-hydroxy-6,7,8-trimethoxynaphthalene

1.2 Other means of identification

Product number -
Other names 4-(3,4-Dimethoxy-phenyl)-1-hydroxy-5,6,7-trimethoxy-naphthalene-2,3-dicarboxylic acid diethyl 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:104756-80-1 SDS

104756-80-1Downstream Products

104756-80-1Relevant academic research and scientific papers

Synthesis and hypolipidemic activity of diesters of arylnaphthalene lignan and their heteroaromatic analogs

Kuroda, Tooru,Kondo, Kazuhiko,Iwasaki, Tameo,Ohtani, Akio,Takashima, Kohki

, p. 678 - 684 (2007/10/03)

A series of diesters of arylnaphthalene lignan and their heteroaromatic analogs were synthesized and evaluated for hypolipidemic activity. The diesters with modifications at C-3 showed excellent hypocholesterolemic and high-density lipoprotein (HDL) cholesterol-elevating activities. Structure- activity analysis indicated that the 2-pyridylmethyl ester 51 has the optimum activity.

Naphthalene derivatives and composition and methods of use, and aldehyde intermediates

-

, (2008/06/13)

Naphthalene derivative of the formula: STR1 wherein R1 is hydrogen atom or a lower alkoxycarbonyl and R2 is a lower alkoxycarbonyl, or R1 and R2 are combined together to form a group of the formula: STR2 each of

Process for preparing a naphthalene derivative

-

, (2008/06/13)

A novel process for preparing a naphthalene derivative of the formula: STR1 wherein R1, R2, R3, R4, R5, R6 and R7 are a lower alkyl group, and an intermediate thereof is disclose

A process for preparing a naphthalene derivative

-

, (2008/06/13)

A novel process for preparing a naphthalene derivative of the formula: wherein R1, R2, R3, R4, R5, R6 and R7 are a lower alkyl group, and an intermediate thereof is disclosed. Said naphthalene derivative (I) and

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