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2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)-, also known as Imidazolidine-2,4-dione, is a chemical compound that belongs to the class of imidazolidine-2,4-diones. It is characterized by its unique structure and properties, including its antibacterial and antifungal capabilities. 2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)is widely used in various industries, particularly in the production of pharmaceuticals and agricultural chemicals, due to its ability to modulate glucose metabolism and its potential applications in treating diabetes and other metabolic disorders.

70974-19-5

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70974-19-5 Usage

Uses

Used in Pharmaceutical Industry:
2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)is used as an active pharmaceutical ingredient for its potential therapeutic applications in treating diabetes and other metabolic disorders. Its ability to modulate glucose metabolism makes it a promising candidate for the development of new drugs targeting these conditions.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals industry, 2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)is used as a biocidal agent due to its antibacterial and antifungal properties. It can be incorporated into various products to protect crops from harmful microorganisms, thereby improving crop yield and quality.
Used in Antimicrobial Applications:
2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)is used as an antimicrobial agent in various consumer products, such as hand sanitizers, surface disinfectants, and personal care products. Its broad-spectrum antimicrobial activity helps to inhibit the growth of bacteria and fungi, providing protection against infections and maintaining hygiene.
Used in Research and Development:
2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)is also used in research and development for studying its potential applications in various fields, including pharmaceuticals, agriculture, and materials science. Researchers are exploring its properties and mechanisms of action to develop new formulations, improve existing products, and discover novel uses for this versatile compound.
However, it is important to note that 2,4-Imidazolidinedione, 5,5-dimethyl-3-(4-fluorophenyl)should be handled with care, as it is considered harmful if ingested and can cause skin and eye irritation upon contact. Proper safety measures and precautions should be taken during its production, use, and disposal to minimize potential risks to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 70974-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70974-19:
(7*7)+(6*0)+(5*9)+(4*7)+(3*4)+(2*1)+(1*9)=145
145 % 10 = 5
So 70974-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H11FN2O2/c1-11(2)9(15)14(10(16)13-11)8-5-3-7(12)4-6-8/h3-6H,1-2H3,(H,13,16)

70974-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-fluorophenyl)-5,5-dimethylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names -

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:70974-19-5 SDS

70974-19-5Downstream Products

70974-19-5Relevant academic research and scientific papers

N1- and N3-Arylations of Hydantoins Employing Diaryliodonium Salts via Copper(I) Catalysis at Room Temperature

Abha Saikia, Raktim,Barman, Dhiraj,Dutta, Anurag,Jyoti Thakur, Ashim

, p. 400 - 410 (2020/12/17)

Copper(I)-catalyzed N-arylation (both N1- and N3-) of hydantoins with diaryliodonium salts as aryl partners at room temperature is reported. The transformation allows diverse scopes on both hydantoins and diaryliodonium salts deliver

3-Arylhydantoine, a class of schistosomicidal compounds

Link,Stohler

, p. 261 - 265 (2007/10/02)

A series of derivatives of 3-arylhydantoin was synthesized and submitted to a broad pharmacological screening. Unexpectedly, some of the tested compounds showed interesting activity against infection with Schistosoma mansoni. From a study on structure-act

Antiandrogenic and schistosomicidal imidazolidine derivatives

-

, (2008/06/13)

Imidazolidine derivatives, as well as processes for their preparation, which have antiandrogenic and schistosomicidal activity.

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