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N-(3,5-dichlorophenyl)-N-(tetrahydro-2,5-dioxo-3-furanyl)Acetamide, commonly referred to as TDFM, is a chemical compound that falls under the category of acetamides. It is characterized by its antifungal and antibacterial properties, which have positioned it as a promising candidate in pharmaceutical research and drug development. TDFM's unique molecular structure also makes it an intriguing subject for further exploration in medicinal chemistry, highlighting its potential as a versatile compound with applications in the medical field.

132689-81-7

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132689-81-7 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
TDFM is utilized as a potential agent for treating a variety of diseases and conditions due to its antifungal and antibacterial properties. Its effectiveness in combating fungal and bacterial infections makes it a valuable component in the development of new medications aimed at improving public health.
Used in Medicinal Chemistry:
The distinctive molecular structure of TDFM makes it an interesting candidate for study in the field of medicinal chemistry. Researchers are likely to investigate its properties further to uncover additional applications and enhance its potential as a therapeutic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 132689-81-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,8 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132689-81:
(8*1)+(7*3)+(6*2)+(5*6)+(4*8)+(3*9)+(2*8)+(1*1)=147
147 % 10 = 7
So 132689-81-7 is a valid CAS Registry Number.

132689-81-7Relevant academic research and scientific papers

2-Carboxytetrahydroquinolines. Conformational and Stereochemical Requirements for Antagonism of the Glycine Site on the NMDA Receptor

Carling, Robert W.,Leeson, Paul D.,Moseley, Angela M.,Baker, Raymond,Foster, Alan C.,et al.

, p. 1942 - 1953 (2007/10/02)

2-Carboxy-1,2,3,4-tetrahydroquinoline derivatives, derived from kynurenic acid, have been synthesized and evaluated for in vitro antagonist activity at the glycine site on the NMDA receptor. 2,3-Dihydrokynurenic acids show reduced potency relative to the

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