Welcome to LookChem.com Sign In|Join Free
  • or
3-Benzylpyrimidin-4(3H)-one is a heterocyclic organic compound with the molecular formula C11H10N2O. It is a derivative of pyrimidin-4(3H)-one, featuring a benzyl group attached to the 3-position of the pyrimidine ring. 3-benzylpyrimidin-4(3H)-one is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various biologically active molecules. The benzyl group's presence can influence the compound's lipophilicity and steric properties, which may be crucial for its interaction with biological targets. 3-Benzylpyrimidin-4(3H)-one can be synthesized through various chemical reactions, such as condensation of appropriate precursors, and is often used as an intermediate in the preparation of more complex pyrimidine-based compounds with potential therapeutic applications.

6146-23-2

Post Buying Request

6146-23-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6146-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6146-23-2 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 6146-23:
(6*6)+(5*1)+(4*4)+(3*6)+(2*2)+(1*3)=82
82 % 10 = 2
So 6146-23-2 is a valid CAS Registry Number.

6146-23-2SDS

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-benzylpyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 3-benzyl-4-pyrimidone

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:6146-23-2 SDS

6146-23-2Relevant academic research and scientific papers

Ortho-Directed Palladium-Catalyzed Direct C-H Functionalization of 3-Picolinyl- A nd 3-(2-Cyanoethyl)pyrimidin-4(3 H)-ones with Aryl Halides

Baudequin, Christine,Bischoff, Laurent,Diallo, Thierno Mamoudou,Frippiat, Steven,Hoarau, Christophe,Levacher, Vincent,Mohamed-Cherif, Anissa,Muselli, Micka?l,Ruiz, Sandra Collado

, p. 1185 - 1190 (2020)

The ortho-directed palladium-catalyzed direct C-H arylation of 3-picolinylpyrimidin-4-one was achieved by using various aryl halides. The method was extended to C-H arylation of pyrimidin-4-ones containing a methoxy group and an aryl group at the C5 site. The 2-cyanoethyl substituent was also evaluated as an ortho-directing group. The method gives access to novel N-substituted 2-aryl or 2,5-diaryl pyrimidin-4-ones. A standard three-step deprotection sequence for the picolinyl group was also studied.

Fe nano particles mediated C-N bond-forming reaction: Regioselective synthesis of 3-[(2-chloroquinolin-3-yl)methyl]pyrimidin-4(3H)ones

Roopan, Selvaraj Mohana,Khan, Fazlur Rahman Nawaz,Mandal, Badal Kumar

, p. 2309 - 2311 (2010)

An efficient and regioselective N-alkylation of 4(3H)-pyrimidone with various electrophiles in the presence of Fe nano particle is reported. The catalyst initiates N-alkylation of amides by alkyl chlorides. The reaction of equimolar 4(3H)-pyrimidone and 2

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6146-23-2