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2(1H)-Quinoxalinone, 5-chloro-3,4-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

148010-70-2

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148010-70-2 Usage

Type of compound

Heterocyclic compound

Structure

Contains a quinoxaline ring

Substitution

Chlorine atom at the 5th position, dihydro group at the 3rd and 4th positions

Potential applications

Pharmaceutical research and drug development

Use

Building block for the synthesis of novel pharmaceutical compounds or starting point for drug discovery efforts

Importance

Unique structural features and potential biological activities make it an interesting and important compound for researchers in the fields of chemistry and pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 148010-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,0,1 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 148010-70:
(8*1)+(7*4)+(6*8)+(5*0)+(4*1)+(3*0)+(2*7)+(1*0)=102
102 % 10 = 2
So 148010-70-2 is a valid CAS Registry Number.

148010-70-2SDS

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 5-chloro-3,4-dihydro-1H-quinoxalin-2-one

1.2 Other means of identification

Product number -
Other names 5-chloro-1,2,3,4-tetrahydroquinoxalin-2-one

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:148010-70-2 SDS

148010-70-2Relevant academic research and scientific papers

High-affinity partial agonist imidazo[1,5-a]quinoxaline amides, carbamates, and ureas at the γ-aminobutyric acid A/benzodiazepine receptor complex

Jacobsen, E. Jon,TenBrink, Ruth E.,Stelzer, Lindsay S.,Belonga, Kenneth L.,Carter, Donald B.,Im, Haesook K.,Im, Wha Bin,Sethy, Vimala H.,Tang, Andy H.,VonVoigtlander, Philip F.,Petke, James D.

, p. 158 - 175 (1996)

A series of imidazo[1,5-a]quinoxaline amides, carbamates, and ureas which have high affinity for the γ-aminobutyric acid A/benzodiazepine receptor complex was developed. Compounds within this class have varying efficacies ranging from antagonists to full

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