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dimethyl 4-(3,4-dimethoxyphenyl)-1-hydroxy-5,6,7-trimethoxynaphthalene-2,3-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104756-72-1

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104756-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104756-72-1 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, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104756-72:
(8*1)+(7*0)+(6*4)+(5*7)+(4*5)+(3*6)+(2*7)+(1*2)=121
121 % 10 = 1
So 104756-72-1 is a valid CAS Registry Number.

104756-72-1SDS

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 dimethyl 4-(3,4-dimethoxyphenyl)-1-hydroxy-5,6,7-trimethoxynaphthalene-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names TA 7552

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:104756-72-1 SDS

104756-72-1Relevant academic research and scientific papers

Arylnaphthalene lignans as novel series of hypolipidemic agents raising high-density lipoprotein level

Iwasaki,Kondo,Nishitani,Kuroda,Hirakoso,Ohtani,Takashima

, p. 1701 - 1705 (2007/10/03)

A series of arylnaphthalene lignans were synthesized and tested for hypolipidemic activity. The most potent compound (4b) (TA-7552) not only reduced serum cholesterol, but also increased high-density lipoproteins cholesterol in rats. The effective dose 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

Process for preparing a naphthalene derivative and a synthetic intermediate thereof

-

, (2008/06/13)

A novel process for preparing a naphthalene derivative of the formula: STR1 wherein R1 and R2 are a lower alkoxycarbonyl group or both may combine to form a group of the formula STR2 one of R3 and R4 is hydrogen

A process for preparing naphthalene derivatives

-

, (2008/06/13)

A novel process for preparing a naphthalene derivative of the formula: wherein each of R1 and R2 is a lower alkyl group; one of R3 and R4 is hydrogen atom or a lower alkoxy group and the other is a lower alkoxy group; and Ring A is a substitute

Novel naphthalene derivative

-

, (2008/06/13)

Naphthalene derivative of the formula: STR1 wherein Ring A is a substituted or unsubstituted benzene ring; each of R1 and R2 is a group of the formula: --OR5, --NHR5 or STR2 or either one of R1 and R

Alkoxynaphthalene derivatives

-

, (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

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