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2-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine is a chemical compound with the molecular formula C12H14N4. It belongs to the class of organic compounds known as cyclopenta[d]pyrimidines, which are heterocyclic compounds with a pyrimidine ring fused to a cyclopentane ring. This specific compound features a phenyl group attached to the cyclopentane ring and an amine functional group at the 4-position of the pyrimidine ring. It is a white crystalline solid and is used as a building block in the synthesis of various pharmaceuticals and agrochemicals, particularly those with potential biological activity. The compound's structure and properties make it a valuable intermediate in the development of new drugs and other chemical products.

7252-78-0

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7252-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7252-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7252-78:
(6*7)+(5*2)+(4*5)+(3*2)+(2*7)+(1*8)=100
100 % 10 = 0
So 7252-78-0 is a valid CAS Registry Number.

7252-78-0SDS

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 2-phenyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine

1.2 Other means of identification

Product number -
Other names 2-phenyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ylamine

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:7252-78-0 SDS

7252-78-0Downstream Products

7252-78-0Relevant academic research and scientific papers

Temperature controlled condensation of nitriles: Efficient and convenient synthesis of β-enaminonitriles, 4-aminopyrimidines and 4-amidinopyrimidines in one system

Li, Yinghua,Zhu, Yingzu,Xiang, Shiqun,Fan, Weibin,Jin, Jiang,Huang, Deguang

, p. 6576 - 6583 (2020/02/25)

A series of β-enaminonitriles, 4-aminopyrimidines and 4-amidinopyrimidines were synthesized by condensation of organonitriles in one system. A wide variety of compounds were obtained in good to excellent yields by simply controlling the reaction temperature. The base-induced transformation process is easy for production. The scope and versatility of the method have been successfully demonstrated with 72 examples. The flexible and diversified characteristics of nitriles were introduced based on electronic effect, steric effect, position of substituted groups and intermolecular hydrogen bonding. An updated reaction mechanism is proposed based on the study of the stoichiometric reaction conditions at variable temperature, and on the investigation of products with cis-trans configuration transformation.

Base-catalyzed synthesis of bicyclic 4-aminopyrimidines from the reaction of dinitriles with mononitriles

Chercheja, Serghei,Simpson, Juliet K.,Lam, Hon Wai

experimental part, p. 3839 - 3845 (2011/06/21)

A convenient method for the synthesis of bicyclic 4-aminopyrimidines is described, involving the reaction of dinitriles with mononitriles in the presence of catalytic potassium tert-butoxide. These reactions proceed via the Thorpe-Ziegler cyclization of t

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