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3-Ethylpyrimidin-4(3H)-one is a heterocyclic organic compound with the molecular formula C6H7N3O. It is a derivative of pyrimidin-4(3H)-one, featuring an ethyl group attached to the 3-position of the pyrimidine ring. 3-ethylpyrimidin-4(3H)-one is a white crystalline solid and is soluble in common organic solvents such as ethanol, methanol, and acetonitrile. It is synthesized through various chemical reactions, including condensation of ethyl acetoacetate with urea or thiourea. 3-Ethylpyrimidin-4(3H)-one is a key intermediate in the synthesis of various pyrimidine-based pharmaceuticals and agrochemicals, such as antifungal agents, antiviral drugs, and herbicides. Its chemical properties include reactivity towards nucleophilic substitution, electrophilic substitution, and oxidation, making it a versatile building block in organic synthesis.

6146-22-1

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6146-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6146-22-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6146-22:
(6*6)+(5*1)+(4*4)+(3*6)+(2*2)+(1*2)=81
81 % 10 = 1
So 6146-22-1 is a valid CAS Registry Number.

6146-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylpyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 3-ethyl-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6146-22-1 SDS

6146-22-1Upstream product

6146-22-1Downstream Products

6146-22-1Relevant academic research and scientific papers

Manganese-Promoted Regioselective Direct C3-Phosphinoylation of 2-Pyridones

Chantarojsiri, Teera,Kittikool, Tanakorn,Phakdeeyothin, Kunita,Yotphan, Sirilata

supporting information, p. 3071 - 3078 (2021/07/22)

A highly efficient and regioselective manganese-induced radical oxidative direct C?P bond formation between 2-pyridones and secondary phosphine oxides was developed. The C3-selective phosphinoylation was conveniently achieved through a combination of substoichiometric manganese and persulfate oxidant under mild conditions. Various 3-phosphinoylated pyridone products can be obtained in moderate to high yields. Preliminary mechanistic studies suggest that the reaction is likely to involve a radical pathway induced by catalytically active Mn3+ species.

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