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169384-56-9

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169384-56-9 Usage

General Description

Methyl N-Cbz-2-piperidineacetate is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is a derivative of piperidine and is often employed as a building block in the creation of various pharmaceuticals and fine chemicals. The compound is known for its ability to act as a protecting group for amines, which can help to facilitate specific reactions in organic synthesis. Its unique structure and reactivity make it a valuable tool for chemists to create complex organic molecules with specific functional groups. Overall, Methyl N-Cbz-2-piperidineacetate plays an important role in the field of organic chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 169384-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,8 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169384-56:
(8*1)+(7*6)+(6*9)+(5*3)+(4*8)+(3*4)+(2*5)+(1*6)=179
179 % 10 = 9
So 169384-56-9 is a valid CAS Registry Number.

169384-56-9SDS

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 benzyl 2-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-N-CBZ-2-METHOXYCARBONYLMETHYL-PIPERIDINE

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:169384-56-9 SDS

169384-56-9Relevant articles and documents

Chemoenzymatic approach to enantiopure piperidine-based β-amino esters in organic solvents

Liljeblad, Arto,Kavenius, Hanna-Maija,Taehtinen, Petri,Kanerva, Liisa T.

, p. 181 - 191 (2007/10/03)

This research concentrates on the enantioselectivities of lipase-catalysed reactions with methyl esters of 2-piperidylacetic acid and 3-piperidinecarboxylic acid derivatives. N-Acetylated 2-piperidylacetic acid methyl ester displayed good enantioselectivi

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