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134516-99-7

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  • Diimidazo[1,5-a:1',2'-c]quinazoline,11-chloro-5-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-2,3-dihydro-

    Cas No: 134516-99-7

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134516-99-7 Usage

Uses

U 90042 is a sedative and hypnotic compound that interacts differentially with the GABAA receptor subtypes.

Biological Activity

GABA A receptor ligand that binds with comparable affinities to three receptor subtypes: α 1 β 2 γ 2 , α 3 β 2 γ 2 and α 6 β 2 γ 2 (K i values are 7.8, 9.5 and 11.0 nM respectively). Potentiates GABA-induced chloride currents in α 6 β 2 γ 2 receptors. Sedative/hypnotic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 134516-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,1 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134516-99:
(8*1)+(7*3)+(6*4)+(5*5)+(4*1)+(3*6)+(2*9)+(1*9)=127
127 % 10 = 7
So 134516-99-7 is a valid CAS Registry Number.

134516-99-7SDS

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 (S)-(-)-Atenolo

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:134516-99-7 SDS

134516-99-7Downstream Products

134516-99-7Relevant articles and documents

Heterocyclic compounds and their preparation and use

-

, (2008/06/13)

New imidazoquinazoline compounds having the general formula STR1 wherein A together with the α-marked carbon atom and the β-marked nitrogen atom is one of the groups STR2 wherein R4, R5, R6 and R7 independently are hydrogen, halogen C1-6 -alkyl, aryl or aralkyl R1 is STR3 cyano or CO2 R8, wherein R8 is hydrogen, C1-6 -alkyl or C3-7 -cycloalkyl, trifluoromethyl or C1-6 -alkoxymethyl, R2 and R3 independently are hydrogen, halogen, CN, C1-6 -alkyl, C2-6 -alkenyl, C2-6 -alkynyl, trifluoromethyl, C1-6 -alkoxy, dialkylaminoalkoxy, aralkoxy, aryloxy which may be substituted with halogen or alkoxy, a cyclic amino group, or NR9 R10, wherein R9 and R10 independently are hydrogen or C1-6 -alkyl. The compounds are useful in psychopharmaceutical preparations as anticonvusants, anxiolytics, hypnotics, antipsychotics, antiemetics, or in improving the cognitive function of the brain of mammals.

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