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ethyl 4-amino-1-benzylpiperidine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

892863-69-3

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892863-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 892863-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,8,6 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 892863-69:
(8*8)+(7*9)+(6*2)+(5*8)+(4*6)+(3*3)+(2*6)+(1*9)=233
233 % 10 = 3
So 892863-69-3 is a valid CAS Registry Number.

892863-69-3SDS

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 ethyl 4-amino-1-benzylpiperidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names rac-4-Amino-1-benzyl-piperidine-3-carboxylic acid ethyl 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:892863-69-3 SDS

892863-69-3Relevant academic research and scientific papers

ANTIBACTERIAL COMPOUNDS HAVING BROAD SPECTRUM OF ACTIVITY

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Page/Page column 118-119; 115, (2016/07/05)

The present invention relates to novel antibacterial compounds, pharmaceutical compositions containing them and their use as antimicrobials.

Synthesis of new trisubstituted 4-aminopiperidines as PAF-receptor antagonists

Benmehdi, Houcine,Lamouri, Aazdine,Serradji, Nawal,Pallois, Frederique,Heymans, Francoise

, p. 299 - 307 (2008/09/18)

Two novel classes of 4-aminopiperidines substituted in the 3-position by groups bearing either a carbamate or a ureido function have been synthesized from ethyl 4-oxo-3-piperidinecarboxylate and 3,3′-iminobis(propanenitrile) , respectively. The key step in this synthesis, the reduction of the piperidinic β-enamino ester or nitrile, occurred readily. In contrast to published works, the free primary amines could be isolated from the corresponding β-amino ester or nitrile. Regioselective amidification of the amino group offered two pairs of diastereoisomers which were successfully separated and identified. Measurement of PAF-receptor antagonist activity gave interesting results with an IC50 close to the micromolar. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

4-Aminopiperidine derivatives

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Page/Page column 19, (2010/11/08)

The present invention relates to compounds of the formula (I) wherein R1 and R2 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases which are associated with DPP-IV, such as diabetes, non-insulin dependent diabetes mellitus and/or impaired glucose tolerance, obesity, and/or metabolic syndrome or β-cell protection.

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