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2(1H)-Pyrimidinone, 4-methyl-6-[2-(4-methylphenyl)ethyl]-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93269-33-1

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93269-33-1 Usage

Core structure

pyrimidinone

Side chain

4-methyl-6-[2-(4-methylphenyl)ethyl]-1-phenyl-

Type of compound

heterocyclic

Potential applications

pharmaceutical

Biological activity

possible

Investigation for therapeutic effects

ongoing

Chemical properties and reactivity

useful in organic synthesis and chemical compound development

Unique structure

The compound has a distinct pyrimidinone core structure with a specific side chain attached to it.

Heterocyclic nature

The presence of a pyrimidinone ring makes the compound heterocyclic, which may contribute to its potential pharmaceutical applications.

Ongoing research

Further studies are needed to fully understand the compound's potential uses and properties, including its biological activity and therapeutic effects in various medical conditions.

Organic synthesis and chemical compound development

The compound's chemical properties and reactivity may make it a valuable building block or intermediate in the synthesis of new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 93269-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93269-33:
(7*9)+(6*3)+(5*2)+(4*6)+(3*9)+(2*3)+(1*3)=151
151 % 10 = 1
So 93269-33-1 is a valid CAS Registry Number.

93269-33-1Downstream Products

93269-33-1Relevant academic research and scientific papers

The Regioselective alkylation of 4,6-Dimethyl-1-phenyl-2(1H)-pyrimidinone

Katoh, Akira,Omote, Yoshimori,Kashima, Choji

, p. 915 - 916 (2007/10/02)

4,6-Dimethyl-1-phenyl-2(1H)-pyrimidinone (I) was treated with alkyl halides in the presence of sodium hydride at low temperature to afford only C-6 alkylated products III and IV in good yields.Further, the mono-, IIIa-d, and di-alkylated 2(1H)-pyrimidinon

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