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4-Pyrimidinamine, 2,6-di-1H-pyrazol-1-yl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

912940-80-8

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912940-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 912940-80-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,2,9,4 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 912940-80:
(8*9)+(7*1)+(6*2)+(5*9)+(4*4)+(3*0)+(2*8)+(1*0)=168
168 % 10 = 8
So 912940-80-8 is a valid CAS Registry Number.

912940-80-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis(1H-pyrazol-1-yl)pyrimidin-4-ylamine

1.2 Other means of identification

Product number -
Other names 4-Pyrimidinamine, 2,6-di-1H-pyrazol-1-yl-

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:912940-80-8 SDS

912940-80-8Downstream Products

912940-80-8Relevant academic research and scientific papers

2-Amino-N-pyrimidin-4-ylacetamides as A2A receptor antagonists: 1. Structure-activity relationships and optimization of heterocyclic substituents

Slee, Deborah H.,Chen, Yongsheng,Zhang, Xiaohu,Moorjani, Manisha,Lanier, Marion C.,Lin, Emily,Rueter, Jaimie K.,Williams, John P.,Lechner, Sandra M.,Markison, Stacy,Malany, Siobhan,Santos, Mark,Gross, Raymond S.,Jalali, Kayvon,Sai, Yang,Zuo, Zhiyang,Yang, Chun,Castro-Palomino, Julio C.,Crespo, María I.,Prat, Maria,Gual, Silvia,Díaz, José-Luis,Saunders, John

, p. 1719 - 1729 (2008)

Previously we have described a novel series of potent and selective A 2A receptor antagonists (e.g., 1) with excellent aqueous solubility.1 While these compounds are efficacious A2A antagonists in vivo, the presence of an

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