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942142-76-9

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942142-76-9 Usage

General Description

(R)-tert-butyl 3-((R)-(3-chlorophenyl)(2-ethoxy-2-oxoethoxy)methyl)piperidine-1-carboxylate is a compound that belongs to the class of organic compounds known as tert-butyl esters. It is a synthetic chemical that is made up of a piperidine ring attached to a 3-chlorophenyl group and an ethoxy-oxoethoxy-methyl side chain. (R)-tert-butyl 3-((R)-(3-chlorophenyl)(2-ethoxy-2-oxoethoxy)methyl)piperidine-1-carboxylate has potential applications in the pharmaceutical and agrochemical industries, and it may be used as an intermediate in the synthesis of various drugs and other biologically active molecules. However, due to its complex structure and potential reactivity, it requires careful handling and proper safety precautions when being utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 942142-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,1,4 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 942142-76:
(8*9)+(7*4)+(6*2)+(5*1)+(4*4)+(3*2)+(2*7)+(1*6)=159
159 % 10 = 9
So 942142-76-9 is a valid CAS Registry Number.

942142-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl (3R)-3-[(R)-(3-chlorophenyl)(2-ethoxy-2-oxoet hoxy)methyl]-1-piperidinecarboxylate

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:942142-76-9 SDS

942142-76-9Downstream Products

942142-76-9Relevant articles and documents

Discovery of VTP-27999, an alkyl amine renin inhibitor with potential for clinical utility

Jia, Lanqi,Simpson, Robert D.,Yuan, Jing,Xu, Zhenrong,Zhao, Wei,Cacatian, Salvacion,Tice, Colin M.,Guo, Joan,Ishchenko, Alexey,Singh, Suresh B.,Wu, Zhongren,McKeever, Brian M.,Bukhtiyarov, Yuri,Johnson, Judith A.,Doe, Christopher P.,Harrison, Richard K.,McGeehan, Gerard M.,Dillard, Lawrence W.,Baldwin, John J.,Claremon, David A.

, p. 747 - 751 (2011/12/01)

Structure guided optimization of a series of nonpeptidic alkyl amine renin inhibitors allowed the rational incorporation of additional polar functionality. Replacement of the cyclohexylmethyl group occupying the S1 pocket with a (R)-(tetrahydropyran-3-yl)

RENIN INHIBITORS

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Page/Page column 32, (2010/08/07)

Disclosed are aspartic protease inhibitors represented by the following structural formula: and pharmaceutically acceptable salts thereof. These compounds are orally active and bind to aspartic proteases to inhibit their activity. They are useful in the t

PIPERIDINE AND MORPHOLINE RENIN INHIBITORS

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Page/Page column 134, (2008/06/13)

Described are compounds which are orally active and bind to renin to inhibit its activity. They are useful in the treatment or amelioration of diseases associated with renin activity. Also described are methods of use of these compounds for treating or ameliorating a renin mediated disorder in a subject.

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