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1H-Indole-2-carboxylic acid, 3-[(3-methoxyphenyl)thio]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

718614-76-7

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718614-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 718614-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,8,6,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 718614-76:
(8*7)+(7*1)+(6*8)+(5*6)+(4*1)+(3*4)+(2*7)+(1*6)=177
177 % 10 = 7
So 718614-76-7 is a valid CAS Registry Number.

718614-76-7Downstream Products

718614-76-7Relevant academic research and scientific papers

Catalytic Synthesis of 3-Thioindoles Using Bunte Salts as Sulfur Sources under Metal-Free Conditions

Qi, Hong,Zhang, Tongxin,Wan, Kefeng,Luo, Meiming

, p. 4262 - 4268 (2016)

An efficient catalytic method for the synthesis of 3-thioindoles has been successfully developed, which uses odorless, stable, readily available crystalline Bunte salts as the sulfenylating agents, iodine as nonmetallic catalyst, and DMSO as both the oxid

1-Benzyl-3-thioaryl-2-carboxyindoles as potent non-peptide endothelin antagonists

Bunker, Amy M.,Edmunds, Jeremy J.,Berryman, Kent A.,Walker, Donnelle M.,Flynn, Michael A.,Welch, Kathy M.,Doherty, Annette M.

, p. 1367 - 1370 (1996)

Endothelin-1 is a potent vasoconstrictor which is thought to be involved in many human disease states. We have developed a series of indole non- peptide endothelin antagonists which display nanomolar receptor affinity. The representative compound from thi

Preparation method of 3-indole thioether

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Paragraph 0015, (2016/10/08)

According to the invention, Bunte salt is employed as a sulfur source to prepare 3-indole thioether. At a certain temperature, elementary iodine or hydroiodic acid and salts thereof is employed as a catalyst, dimethyl sulfoxide is employed as an oxidant,

3-Sulfenylation of indole-2-carboxylates

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Page 8, (2010/02/07)

A highly efficient one-pot procedure for 3-sulfenilation of indole 2-carboxylates is described. Treatment of thiols with N-chlorosuccinimide at -78° C. in CH2Cl2 affords sulfenyl chlorides in situ that readily react with indole 2-carboxylates to give 3-th

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