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219832-76-5

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219832-76-5 Usage

General Description

4-Piperidineacetic acid, .alpha.-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester is a chemical compound that belongs to the family of piperidine carboxylic acids. It is known for its use as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. 4-Piperidineacetic acid, .alpha.-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester is often employed as a building block in the production of various drugs, including antipsychotic and anticonvulsant medications. Additionally, it has been utilized in the development of insecticides and herbicides. The methyl ester form of this chemical offers stability and facilitates its use in various chemical reactions for the creation of other compounds with specific chemical properties and functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 219832-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 219832-76:
(8*2)+(7*1)+(6*9)+(5*8)+(4*3)+(3*2)+(2*7)+(1*6)=155
155 % 10 = 5
So 219832-76-5 is a valid CAS Registry Number.

219832-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-piperidin-4-ylacetate

1.2 Other means of identification

Product number -
Other names tert-Butoxycarbonylamino-piperidin-4-yl-acetic 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:219832-76-5 SDS

219832-76-5Relevant articles and documents

Potent and selective bicyclic lactam inhibitors of thrombin: Part 2:P1 modifications

Plummer, Janet S.,Berryman, Kent A.,Cai, Cuiman,Cody, Wayne L.,Dimaio, John,Doherty, Annette M.,Edmunds, Jeremy J.,He, John X.,Holland, Debra R.,Levesque, Sophie,Kent, Darin R.,Narasimhan, Lakshmi S.,Rubin, J. Ronald,Rapundalo, Stephen T.,Siddiqui, M. Arshad,Susser, Alan J.,St-Denis, Yves,Winocour, Peter D.

, p. 3409 - 3414 (2007/10/03)

The synthesis and antithrombotic activity of a series of nonpeptide bicyclic thrombin inhibitors is described. We have explored the SAR with modifications to the P1 site. The introduction of arginine mimetics at the P1 site led to potent and selective thrombin inhibitors.

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