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4H-Imidazol-4-one, 3,5-dihydro-5-[(4-methoxyphenyl)methylene]-3-methyl-2-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14748-39-1

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14748-39-1 Usage

Molecular Structure

Contains an imidazol-4-one ring and a 4-methoxyphenyl group.

Functional Groups

Imidazol-4-one ring: This heterocyclic ring consists of four carbon atoms, two nitrogen atoms, and one oxygen atom.
4-methoxyphenyl group: A phenyl group substituted with a methoxy (-OCH3) group at the para position.
Methylthio group: A methyl group (-CH3) attached to a sulfur atom.

Chemical Classification

Thioether due to the presence of the methylthio group.

Biological Activities

Potential for various biological activities.
Application in pharmaceutical research.

Research Status

Interest in organic chemistry and pharmaceutical research.
Requires further research to fully understand chemical properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 14748-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14748-39:
(7*1)+(6*4)+(5*7)+(4*4)+(3*8)+(2*3)+(1*9)=121
121 % 10 = 1
So 14748-39-1 is a valid CAS Registry Number.

14748-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methoxy-benzylidene)-3-methyl-2-methylsulfanyl-3,5-dihydro-imidazol-4-one

1.2 Other means of identification

Product number -
Other names 5-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-3-methyl-2-methylsulfanyl-3,5-dihydro-imidazol-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:14748-39-1 SDS

14748-39-1Relevant academic research and scientific papers

Synthesis of methylsulfanyl analogs of Kaede protein chromophore

Zaitseva, Elvira R.,Smirnov, Alexander Yu.,Shcerbinina, Sofya I.,Zasedateleva, Vlada V.,Mineev, Konstantin S.,Baranov, Mikhail S.

, p. 399 - 402 (2020)

[Figure not available: see fulltext.] 5-Arylidene-1-methyl-2-[2-(methylsulfanyl)-2-phenylethenyl]-1H-imidazol-5(4H)-ones were synthesized as a result of the reaction of 5-arylidene-1-methyl-2-(methylsulfanyl)-1H-imidazol-5(4H)-ones with terminal acetylene

Studies on 5-Arylidene-3-phenyl-2-methylmercaptohydantoins

Kadry, Azza M.,Mansour, Salwa A.

, p. 155 - 157 (2007/10/02)

The action of ammonium acetate on 5-arylidene-3-phenyl-2-methylmercaptohydantoins 1g,h in acetic acid led to the formation of the 5-arylidene-3-phenylhydantoin derivatives 4a,b.In absence of a solvent, ring opening and rearrangement took place with the fo

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