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77472-98-1

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77472-98-1 Usage

Description

Pipequaline is a partial agonist of central benzodiazepine receptors (Ki = 78 nM in a radioligand binding assay). In mice, pipequaline enhances the effects of diazepam , further reducing foot shock-induced fighting behavior and the number of maximal electroshock-induced seizures and potentiating the muscle relaxant and hypnotic effects. Pipequaline also increases drinking in the Vogel punished drinking task indicating anxiolytic-like activity that can be reversed by the benzodiazepine receptor antagonist flumazenil .

Check Digit Verification of cas no

The CAS Registry Mumber 77472-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,7 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77472-98:
(7*7)+(6*7)+(5*4)+(4*7)+(3*2)+(2*9)+(1*8)=171
171 % 10 = 1
So 77472-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H24N2/c1-2-6-18(7-3-1)22-16-19(11-10-17-12-14-23-15-13-17)20-8-4-5-9-21(20)24-22/h1-9,16-17,23H,10-15H2

77472-98-1SDS

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 2-phenyl-4-(2-piperidin-4-ylethyl)quinoline

1.2 Other means of identification

Product number -
Other names Pipequalina

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:77472-98-1 SDS

77472-98-1Upstream product

77472-98-1Downstream Products

77472-98-1Relevant articles and documents

2-(4-Piperidyl)-1-(4-quinolyl)-ethanones and ethanes

-

, (2008/06/13)

Compounds, useful as medicaments, of the formula: STR1 in which R is hydrogen, alkyl, alkenyl or arylalkyl, R1 is hydrogen, alkyl or alkenyl, R2 is hydrogen, alkyl, arylalkyl, phenyl, pyridyl, thienyl or substituted phenyl, X is hydr

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