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217805-63-5

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217805-63-5 Usage

Class

Pyrazole

Structure

A phenyl and pyrrolidinyl group attached to a central pyrazole ring

Therapeutic potential

Treatment of central nervous system disorders such as anxiety, depression, and schizophrenia

Mechanism of action

Modulation of certain neurotransmitters in the brain

Research status

Ongoing to explore its pharmacological properties and potential as a medication for various neurological and psychiatric conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 217805-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,8,0 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 217805-63:
(8*2)+(7*1)+(6*7)+(5*8)+(4*0)+(3*5)+(2*6)+(1*3)=135
135 % 10 = 5
So 217805-63-5 is a valid CAS Registry Number.

217805-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-3-[(2R)pyrrolidinyl]-1H-pyrazole

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:217805-63-5 SDS

217805-63-5Downstream Products

217805-63-5Relevant articles and documents

The design of potent and selective inhibitors of DPP-4: Optimization of ADME properties by amide replacements

Nordhoff, Sonja,Bulat, Stephan,Cerezo-Galvez, Silvia,Hill, Oliver,Hoffmann-Enger, Barbara,Lopez-Canet, Meritxell,Rosenbaum, Claudia,Rummey, Christian,Thiemann, Meinolf,Matassa, Victor G.,Edwards, Paul J.,Feurer, Achim

scheme or table, p. 6340 - 6345 (2010/06/11)

For a series of β-homophenylalanine based inhibitors of dipeptidyl peptidase IV ADME properties were improved by the incorporation of amide replacements. These efforts led to a novel series of potent and selective inhibitors of DPP-4 that exhibit an attractive pharmacokinetic profile and show excellent efficacy in an animal model of diabetes.

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