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methyl 4-chloro-2-(2-(3,5-dimethylphenyl)acetamido)-5-iodobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

199861-83-1

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199861-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199861-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,6 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 199861-83:
(8*1)+(7*9)+(6*9)+(5*8)+(4*6)+(3*1)+(2*8)+(1*3)=211
211 % 10 = 1
So 199861-83-1 is a valid CAS Registry Number.

199861-83-1SDS

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 4-chloro-2-[2-(3,5-dimethylphenyl)-acetylamino]-5-iodo-benzoic acid methyl ester

1.2 Other means of identification

Product number -
Other names 4-Chloro-2-[2-(3,5-dimethyl-phenyl)-acetylamino]-5-iodo-benzoic acid methyl 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:199861-83-1 SDS

199861-83-1Relevant academic research and scientific papers

Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents

Young, Jonathan R.,Huang, Song X.,Chen, Irene,Walsh, Thomas F.,DeVita, Robert J.,Wyvratt Jr., Matthew J.,Goulet, Mark T.,Ren, Ning,Lo, Jane,Yang, Yi Tien,Yudkovitz, Joel B.,Cheng, Kang,Smith, Roy G.

, p. 1723 - 1727 (2007/10/03)

A series of 3-arylquinolones was prepared and evaluated for their ability to act as gonadotropin releasing hormone (GnRH) antagonists. A variety of substitution patterns of the 3-aryl substituent are described. The 3,4,5-trimethylphenyl substituent (23h) was found to be optimal. (C) 2000 Elsevier Science Ltd. All rights reserved.

Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides

Walsh, Thomas F.,Toupence, Richard B.,Young, Jonathan R.,Huang, Song X.,Ujjainwalla, Feroze,Devita, Robert J.,Goulet, Mark T.,Wyvratt Jr., Matthew J.,Fisher, Michael H.,Lo, Jane-Ling,Ren, Ning,Yudkovitz, Joel B.,Yang, Yi Tien,Cheng, Kang,Smith, Roy G.

, p. 443 - 447 (2007/10/03)

SAR studies which focused upon the C-6 position of a recently described series of quinolone gonadotropin releasing hormone antagonists are reported. Synthetic access to diverse quinolone-6-carboxamides was achieved via the palladium-catalyzed amino-carbonylation reactions of iodide 4 with various amines. Amides related to 9y were especially potent, functional antagonists of rat and human GnRH receptors. (C) 2000 Elsevier Science Ltd. All rights reserved.

Antagonists of gonadotropin releasing hormone

-

, (2008/06/13)

PCT No. PCT/US97/08432 Sec. 371 Date Nov. 12, 1998 Sec. 102(e) Date Nov. 12, 1998 PCT Filed May 16, 1997 PCT Pub. No. WO97/44339 PCT Pub. Date Nov. 27, 1997There are disclosed compounds of formula (I) and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related conditions in both men and women.

Antagonists of gonadotropin releasing hormone

-

, (2008/06/13)

PCT No. PCT/US97/08479 Sec. 371 Date Nov. 12, 1998 Sec. 102(e) Date Nov. 12, 1998 PCT Filed May 16, 1997 PCT Pub. No. WO97/44321 PCT Pub. Date Nov. 27, 1997There are disclosed compounds of formula (I) and pharmaceutical acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related conditions.

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