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66548-69-4

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66548-69-4 Usage

Uses

Different sources of media describe the Uses of 66548-69-4 differently. You can refer to the following data:
1. CL 218872 is a useful research chemical. CL 218872 is a putative anxiolytic.
2. CL 218872 is a benzodiazepine receptor (BZR) partial agonist and a putative anxiolytic.

Biological Activity

Benzodiazepine agonist displaying selectivity for α 1 subunit-containing GABA A receptors (K i values are 130, 1820, 1530, > 10000, 490 and > 10000 nM for α 1, α 2, α 3, α 4, α 5 and α 6-subunit containing receptors respectively). Orally active anxiolytic and anticonvulsant in vivo .

Check Digit Verification of cas no

The CAS Registry Mumber 66548-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,4 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66548-69:
(7*6)+(6*6)+(5*5)+(4*4)+(3*8)+(2*6)+(1*9)=164
164 % 10 = 4
So 66548-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H9F3N4/c1-8-17-18-12-6-5-11(19-20(8)12)9-3-2-4-10(7-9)13(14,15)16/h2-7H,1H3

66548-69-4SDS

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 3-methyl-6-[3-(trifluoromethyl)phenyl]-[1,2,4]triazolo[4,3-b]pyridazine

1.2 Other means of identification

Product number -
Other names CL 218,872

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:66548-69-4 SDS

66548-69-4Relevant articles and documents

A New and Improved Synthesis of 6-Aryl-1,2,4-triazolopyridazines

Lieberman, Daniel F.,Albright, J. Donald

, p. 827 - 830 (2007/10/02)

A new and improved synthesis of 6-aryl-1,2,4-triazolopyridazines is described.This methodology provides the title compounds under mild conditions and in high yields.The first step comprises the condensation of an aryl methyl ketone with a 4-amino-1

Method for treating anxiety in mammals

-

, (2008/06/13)

This disclosure describes compositions of matter useful as anxiolytic agents and the method of meliorating anxiety in mammals therewith; the active ingredients of said compositions of matter being certain substituted 6-phenyl-1,2,4-triazolo[4,3-b]pyridazines or the pharmacologically acceptable acid-addition salts thereof.

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