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[1,2,4]Triazolo[1,5-a]quinoxalin-4-amine, 8-chloro-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168210-19-3

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168210-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168210-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,2,1 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168210-19:
(8*1)+(7*6)+(6*8)+(5*2)+(4*1)+(3*0)+(2*1)+(1*9)=123
123 % 10 = 3
So 168210-19-3 is a valid CAS Registry Number.

168210-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-chloro-2-phenyl-[1,2,4]triazolo[1,5-a]quinoxalin-4-amine

1.2 Other means of identification

Product number -
Other names [1,2,4]Triazolo[1,5-a]quinoxalin-4-amine,8-chloro-2-phenyl

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:168210-19-3 SDS

168210-19-3Downstream Products

168210-19-3Relevant academic research and scientific papers

Synthesis of some tricyclic heteroaromatic systems and their A1 and A2a adenosine binding activity

Colotta, V.,Cecchi, L.,Catarzi, D.,Filacchioni, G.,Martini, C.,et al.

, p. 133 - 139 (2007/10/02)

The syntheses, A%1 and A2a adenosine receptor affinities and structure-activity relationships of some 2-aryl-1,2,4-triazoloquinoxalines, 2-arylimidazoquinoxalines, 1-arylimidazoquinoxalines are reported and compared with that of a previously reported 2-phenylpyrazoloquinoxaline.The results show that some triazoloquinoxalines are potent and specific A1 adenosine receptor ligands and that the replacement of either nitrogen at position 1 or 3 of the triazoloquinoxaline moiety with a CH brought about a decrease in affinity at both adenosine receptors. adenosine receptor ligand / 1,2,4-triazoloquinoxaline / imidazoquinoxaline / imidazoquinoxaline / tricyclic heteroaromatic system

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