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4(3H)-PyriMidinone, 6-aMino-2-(2-furanyl)-, also known as 6-amino-2-(2-furanyl)-4(3H)-pyrimidinone, is a heterocyclic organic compound with the molecular formula C7H7N3O2. It is a derivative of pyrimidinone, featuring a 6-amino group and a 2-furanyl substituent. 4(3H)-PyriMidinone, 6-aMino-2-(2-furanyl)- is of interest in medicinal chemistry and pharmaceutical research due to its potential applications in the development of antiviral and anticancer drugs, as well as its role as a building block in the synthesis of more complex molecules. Its chemical structure and properties make it a valuable intermediate in the synthesis of various biologically active compounds.

67945-75-9

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67945-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67945-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67945-75:
(7*6)+(6*7)+(5*9)+(4*4)+(3*5)+(2*7)+(1*5)=179
179 % 10 = 9
So 67945-75-9 is a valid CAS Registry Number.

67945-75-9SDS

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 6-amino-2-(furan-2-yl)-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-amino-2-furan-2-yl-3H-pyrimidin-4-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

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More Details:67945-75-9 SDS

67945-75-9Relevant academic research and scientific papers

Identification of novel, water-soluble, 2-amino-N-pyrimidin-4-yl acetamides as A2A receptor antagonists with in vivo efficacy

Slee, Deborah H.,Zhang, Xiaohu,Moorjani, Manisha,Lin, Emily,Lanier, Marion C.,Chen, Yongsheng,Rueter, Jaimie K.,Lechner, Sandra M.,Markison, Stacy,Malany, Siobhan,Joswig, Tanya,Santos, Mark,Gross, Raymond S.,Williams, John P.,Castro-Palomino, Julio C.,Crespo, María I.,Prat, Maria,Gual, Silvia,Díaz, José-Luis,Wen, Jenny,O'Brien, Zhihong,Saunders, John

, p. 400 - 406 (2008/12/20)

Potent adenosine hA2A receptor antagonists are often accompanied by poor aqueous solubility, which presents issues for drug development. Herein we describe the early exploration of the structure-activity relationships of a lead pyrimidin-4-yl a

2, 6 BISHETEROARYL-4-AMINOPYRIMIDINES AS ADENOSINE RECEPTOR ANTAGONISTS

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Page/Page column 71, (2010/02/12)

4-Aminopyrimidine derivatives of formula (I) FORMULA heteroaryl groups, including pharmaceutically acceptable salts thereof, wherein R1 and R2 are adenosine A2A receptor antagonists useful in the treatment of movement disorders such as Parkinson's disease.

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