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95629-02-0

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95629-02-0 Usage

General Description

3-Bromo-4-oxo-piperidine-1-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H11BrNO3. It is an ethyl ester derivative of piperidine-1-carboxylic acid and contains a bromine atom and a carbonyl group on the piperidine ring. 3-BROMO-4-OXO-PIPERIDINE-1-CARBOXYLIC ACID ETHYL ESTER can be used in organic synthesis and pharmaceutical research as a building block for the synthesis of various piperidine derivatives. It is also a potential precursor in the production of pharmaceuticals and agrochemicals. The chemical properties and reactivity of 3-bromo-4-oxo-piperidine-1-carboxylic acid ethyl ester allow for its use in the development of biologically active compounds for a variety of applications.

Check Digit Verification of cas no

The CAS Registry Mumber 95629-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95629-02:
(7*9)+(6*5)+(5*6)+(4*2)+(3*9)+(2*0)+(1*2)=160
160 % 10 = 0
So 95629-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12BrNO3/c1-2-13-8(12)10-4-3-7(11)6(9)5-10/h6H,2-5H2,1H3

95629-02-0SDS

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 ethyl 3-bromo-4-oxopiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 3-bromo-4-oxo-piperidine-1-carboxylate

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:95629-02-0 SDS

95629-02-0Relevant articles and documents

Further optimization of the mGlu5 PAM clinical candidate VU0409551/JNJ-46778212: Progress and challenges towards a back-up compound

Zhou, Ya,Malosh, Chrysa,Conde-Ceide, Susana,Martínez-Viturro, Carlos Manuel,Alcázar, Jesus,Lavreysen, Hilde,Mackie, Claire,Bridges, Thomas M.,Daniels, J. Scott,Niswender, Colleen M.,Jones, Carrie K.,Macdonald, Gregor J.,Steckler, Thomas,Conn, P. Jeffrey,Stauffer, Shaun R.,Bartolomé-Nebreda, José Manuel,Lindsley, Craig W.

, p. 3515 - 3519 (2015/08/06)

This Letter describes the progress and challenges in the continued optimization of the mGlu5 positive allosteric modulator (PAM) clinical candidate VU0490551/JNJ-46778212. While many analogs addressed key areas for improvement, no one compound possessed the amalgamation of improvements needed within the (2(phenoxymethyl)-6,7-dihydrooxazolo[5,4-c]pyridine-5(4H)-yl(aryl)methanone scaffold to advance as a back-up clinical candidate. However, many analogs displayed excellent solubility and physiochemical properties, and were active in the amphetamine-induced hyperlocomotion (AHL) model. Moreover, the SAR was robust for this series of PAMs, and both polar and hydrogen-bond donors were found to be tolerated, leading to analogs with overall attractive profiles and good ligand efficiencies. Graphical abstract

SUBSTITUTED SULFONAMIDE DERIVATIVES

-

Page/Page column 143, (2009/11/29)

The invention relates to substituted sulfonamide derivatives, processes for the preparation thereof, medicaments containing these compounds and the use of substituted sulfonamide derivatives for the preparation of medicaments.

N-acylamino acid amide compounds and intermediates for preparation thereof

-

, (2008/06/13)

The present invention discloses the compound represented by the formula (I): wherein A represents the following formula (a-1) or the following formula (a-2): B represents the following formula (b): (wherein the symbols are each as defined in the specification) or a pharmaceutically acceptable salts thereof, and intermediates for the preparation thereof, which have excellent platelet aggregation inhibitory activity and other properties and useful as prophylactic or therapeutic agents for diseases associated with a fibrinogen receptor, thrombosis, infarction and the like.

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