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2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methyl-, is a heterocyclic compound characterized by the fusion of an indole ring and an imidazolidinedione ring. This unique structure endows the compound with aromatic properties from the indole ring and stability and reactivity from the imidazolidinedione ring. The presence of a methyl group at the 3-position of the imidazolidinedione ring further modulates the compound's properties and reactivity, making it a versatile chemical building block with potential applications in various fields.

200804-97-3

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200804-97-3 Usage

Uses

Used in Pharmaceutical Synthesis:
2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methylis used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. The combination of indole and imidazolidinedione moieties in the compound imparts valuable biological activities to the resulting compounds, making it a promising candidate for the development of new drugs.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methylis utilized for its potential to contribute to the discovery of new drugs. The presence of both indole and imidazolidinedione moieties allows for the exploration of various chemical modifications and the development of compounds with specific therapeutic properties.
Used in Drug Discovery:
2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methylplays a crucial role in drug discovery, as its unique structure and properties can be leveraged to identify and optimize potential drug candidates. 2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methyl-'s versatility and reactivity make it an attractive building block for the design and synthesis of novel therapeutic agents.
Overall, 2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methylis a valuable chemical compound with a wide range of applications in the pharmaceutical industry, medicinal chemistry, and drug discovery. Its unique structure and properties make it a promising building block for the development of innovative and effective therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 200804-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,8,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 200804-97:
(8*2)+(7*0)+(6*0)+(5*8)+(4*0)+(3*4)+(2*9)+(1*7)=93
93 % 10 = 3
So 200804-97-3 is a valid CAS Registry Number.

200804-97-3SDS

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 5-(1H-Indol-3-ylmethylene)-3-methylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Imidazolidinedione, 5-(1H-indol-3-ylmethylene)-3-methyl-

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:200804-97-3 SDS

200804-97-3Upstream product

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