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(3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID is a synthetic chemical compound characterized by a thiazolidine ring structure, which includes an ethyl group, a phenyl group, and an acetic acid group. (3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID has been of interest in pharmaceutical research and development due to its potential as an antitumor, anti-inflammatory, and other pharmacological agents. Thiazolidine derivatives, like (3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID, are being studied for their medicinal properties, although more research is necessary to fully understand and utilize their potential.
Used in Pharmaceutical Research and Development:
(3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID is used as a potential pharmacological agent for its possible antitumor and anti-inflammatory properties. Its unique structure and functional groups may contribute to its therapeutic effects, making it a candidate for further study and development in the field of medicine.
Used in Antitumor Applications:
In the field of oncology, (3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID is being investigated for its potential as an antitumor agent. Its specific mechanism of action and efficacy against various types of cancer are areas of active research, with the aim of identifying its role in cancer treatment and prevention.
Used in Anti-Inflammatory Applications:
(3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID is also being explored for its potential as an anti-inflammatory agent. Its ability to modulate inflammatory responses could make it a valuable tool in the treatment of various inflammatory conditions, pending further research and validation.
Used in Drug Design and Development:
In the pharmaceutical industry, (3-ETHYL-4-OXO-2-PHENYLIMINO-THIAZOLIDIN-5-YL)-ACETIC ACID serves as a starting point for drug design and development. Its unique chemical structure can be modified and optimized to create new compounds with improved pharmacological properties, potentially leading to the discovery of novel therapeutic agents.

104445-59-2

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104445-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104445-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104445-59:
(8*1)+(7*0)+(6*4)+(5*4)+(4*4)+(3*5)+(2*5)+(1*9)=102
102 % 10 = 2
So 104445-59-2 is a valid CAS Registry Number.

104445-59-2Relevant academic research and scientific papers

The Reaction of Thiourea Derivatives with Maleic Acid Anhydride

Zawisza, Tadeusz,Wagner, Edwin

, p. 149 - 158 (2007/10/02)

The reaction of thiourea derivatives with maleic and bromomaleic acid anhydride is described, the chemical structure of the compound obtained is proved; some biologically active acids yield amide derivatives 24-32.Amides of the 1,3-thiazine-6-carboxylic a

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