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Benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester is a chemical compound that belongs to the class of benzo[b]thiophene derivatives. Benzo[b]thiophene-5,6-dicarboxylic acid,
7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester is a dimethyl ester, formed by the condensation of two molecules of methanol with one molecule of the parent compound. It features a hydroxy group, which may contribute to its potential biological activity and pharmacological relevance. The presence of a dimethoxyphenyl group in its structure suggests that Benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester could have antioxidant properties or other health benefits. Further research is required to fully explore the biological properties and potential applications of Benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester.

123716-10-9

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123716-10-9 Usage

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester is used as a potential pharmaceutical candidate for its possible biological activity and pharmacological relevance. The hydroxy group in its structure may contribute to its potential use in the development of new drugs or therapeutic agents.
Used in Antioxidant Applications:
Due to the presence of a dimethoxyphenyl group, benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester is used as an antioxidant in various applications. Its antioxidant properties may provide health benefits and protect against oxidative stress, which is implicated in various diseases and aging processes.
Used in Chemical Research:
Benzo[b]thiophene-5,6-dicarboxylic acid, 7-(3,4-dimethoxyphenyl)-4-hydroxy-, dimethyl ester is used as a research compound in the field of organic chemistry. Its unique structure and potential properties make it an interesting subject for further studies, which could lead to the discovery of new chemical reactions, synthesis methods, or applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 123716-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,1 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123716-10:
(8*1)+(7*2)+(6*3)+(5*7)+(4*1)+(3*6)+(2*1)+(1*0)=99
99 % 10 = 9
So 123716-10-9 is a valid CAS Registry Number.

123716-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-5,6-bis(methoxycarbonyl)-7-(3,4-dimethoxyphenyl)benzo<b>thiophene

1.2 Other means of identification

Product number -
Other names 4-hydroxy-5,6-bis(methoxycarbonyl)-7-(3,4-dimethoxyphenyl)benzo[b]thiophene

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:123716-10-9 SDS

123716-10-9Downstream Products

123716-10-9Relevant 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.

An Efficient Synthesis of Heterocyclic Analogs of 1-Arylnaphthalene Lignans

Kuroda, Tooru,Takahashi, Masami,Ogiku, Tsuyoshi,Ohmizu, Hiroshi,Nishitani, Takashi,et al.

, p. 7353 - 7357 (2007/10/02)

The heterocyclic analogs 5a-f, 16, and 20 of 1-arylnaphthalene lignans were synthesized by Diels-Alder reactions of acetoxy aldehydes 11a-f, 14, and 18 with dimethyl acetylenedicarboxylate.A pathway for formation of 5a-f, 16, and 20 through the intermediacy of heteroaromatic isobenzofurans derived from acetoxy aldehydes is discussed.

A New Method for Generation of 4- and 6-Aryl Thienofurans, and 3-Aryl Furopyridine

Kuroda, Tooru,Takahashi, Masami,Ogiku, Tsuyoshi,Ohmizu, Hiroshi,Kondo, Kazuhiko,Iwasaki, Tameo

, p. 1635 - 1636 (2007/10/02)

6-Aryl thienofurans 2a-c, 4-(3,4-dimethoxyphenyl)thienofuran 3a, and 3-(3,4-dimethoxyphenyl)furopyridine 4a, which were intercepted in situ by dimethyl acetylenedicarboxylate to give the corresponding Diels-Alder adducts in good yield

Phenyl benzothiophene hypolipidemic derivatives

-

, (2008/06/13)

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

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