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174543-82-9

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174543-82-9 Usage

General Description

Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate is a chemical compound with the molecular formula C14H19NO3. It is a derivative of piperidine, which is a heterocyclic amine with various pharmaceutical applications. The "Cbz" in the name refers to the carbobenzyloxy protecting group, which is commonly used in organic synthesis to protect amines. Methyl 1-Cbz-3-Methylpiperidine-3-carboxylate has been studied for its potential use in the synthesis of pharmaceutical compounds and as a building block in organic chemistry. It has also been investigated for its biological activities and potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 174543-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,5,4 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 174543-82:
(8*1)+(7*7)+(6*4)+(5*5)+(4*4)+(3*3)+(2*8)+(1*2)=149
149 % 10 = 9
So 174543-82-9 is a valid CAS Registry Number.

174543-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl 3-methyl 3-methyl-1,3-piperidinedicarboxylate

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:174543-82-9 SDS

174543-82-9Relevant articles and documents

On the Ritter reaction of cyclic hydroxyamines: Synthesis of conformationally-restricted reduced amide dipeptide isosteres

Taylor, G. Mark,Baker, Stewart J.,Gedney, Andrea,Pearson, David J.,Sibley, Graham E. M.

, p. 1297 - 1300 (2007/10/03)

The Ritter reactions of 3-alkyl-3-hydroxyazetidine or -piperidine derivatives give low yields of the desired products, whereas the 3-alkyl-3-hydroxy-pyrrolidine and 4-alkyl-4-hydroxy-piperidine derivatives react smoothly to give the corresponding acetamides. An alternative route to 3-acylamino-3-alkylpiperidines, which were designed as conformationally-restricted reduced amide dipeptide isosteres, was devised from nipecotic acid vai a Hofmann rearrangement.

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