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2-Benzofurancarboxylic acid, 5-[2-[1-(triphenylmethyl)-1H-tetrazol-5-yl]phenyl]-, ethyl ester is a complex organic compound with the molecular formula C31H25N3O3. It is a derivative of benzofurancarboxylic acid, featuring a benzofuran ring and a tetrazol-5-yl group attached to a phenyl moiety. The compound is further characterized by an ethyl ester group, which is a derivative of an acid where the hydroxyl group is replaced by an ethoxy group. This specific chemical structure may have potential applications in various fields, such as pharmaceuticals or materials science, due to its unique properties and reactivity.

188714-62-7

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188714-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188714-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,1 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 188714-62:
(8*1)+(7*8)+(6*8)+(5*7)+(4*1)+(3*4)+(2*6)+(1*2)=177
177 % 10 = 7
So 188714-62-7 is a valid CAS Registry Number.

188714-62-7SDS

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 5-[2-(1-Trityl-1H-tetrazol-5-yl)-phenyl]-benzofuran-2-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names -

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

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More Details:188714-62-7 SDS

188714-62-7Relevant academic research and scientific papers

The conformation and activity relationship of benzofuran derivatives as angiotensin II receptor antagonists

Yoo, Sung-Eun,Lee, Seung-Heui,Kim, Soo-Kyung,Lee, Sung-Hou

, p. 445 - 459 (2007/10/03)

We have synthesized various benzofuran derivatives to study the relationship between the conformation and the angiotensin II type I receptor antagonistic activity.

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