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13797-13-2

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13797-13-2 Usage

Structure

A derivative of piperidine and propanoic acid

Functional groups

Contains a nitrophenyl group

Pharmacological activity

Has potential pharmacological activity

Research and development

Often used in the research and development of drugs

Applications

May have applications in the synthesis of various pharmaceuticals and organic compounds

Unique properties

Unique structure and properties that contribute to its potential applications

Biological activities

May possess biological activities valuable in studying disease mechanisms and developing new therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 13797-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13797-13:
(7*1)+(6*3)+(5*7)+(4*9)+(3*7)+(2*1)+(1*3)=122
122 % 10 = 2
So 13797-13-2 is a valid CAS Registry Number.

13797-13-2SDS

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 α-(p-nitrophenyl)-β-(N-piperidyl)propionic aicd

1.2 Other means of identification

Product number -
Other names 3-(N-Piperidyl)-2-(p-nitrophenyl)propionsaeure

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:13797-13-2 SDS

13797-13-2Relevant articles and documents

Intramolecular Carbenoid Reactions of Pyrrole Derivatives. A Total Synthesis of (+/-)-Ipalbidine

Jefford, Charles W.,Kubota, Tadatoshi,Zaslona, Alexander

, p. 2048 - 2061 (2007/10/02)

A mew method for alkaloid synthesis is described.The rhodium(II)-acetate-catalyzed decomposition of 3-(4-acetoxyphenyl)-1-diazo-4-(pyrrol-1-yl)-2-butanone (5d) gave 6-(4-acetoxyphenyl)-5,6-dihydro-7(8H)-indolizinone (6d) in 82percent yield via an intramolecular carbenoid reaction.The latter compound was converted in four steps in 13percent overall yield to (+/-)-ipalbidine (1b).

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