Citraconic Anhydride

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Identification

Molecular formula
C7H10N2O2S
CAS Number
6651-38-3
IUPAC Name
2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid
Molecular Weight
190.25g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6740g/cm3
Synonyms
3655-88-7
Interesting facts

Interesting Facts About 2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid

The compound 2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid is a fascinating example of heterocyclic chemistry, showcasing the importance of thiazine and thiadiazine structures in medicinal chemistry. Below are some intriguing insights into this compound:

  • Structural Diversity: The compound contains a thiadiazinan ring, which is a six-membered heterocyclic structure that incorporates both sulfur and nitrogen atoms. This structural variety contributes to its unique chemical properties.
  • Potential Biological Activity: Compounds with thiadiazine derivatives have garnered interest due to their potential pharmacological activities, including antimicrobial, anti-inflammatory, and anti-cancer properties.
  • Isolation and Synthesis: The synthesis of 2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid emphasizes the importance of developing efficient synthetic routes for producing heterocyclic compounds that can be utilized in drug development.
  • Synthesis Methodologies: Chemists utilize various methods for synthesizing this compound, including cyclization reactions that allow for the incorporation of the sulfur and nitrogen framework into organic molecules.

As researchers continue to unlock the potential of such chemical entities, compounds like 2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid remain key players in the quest for new therapeutic agents. The exploration of their biological and chemical properties is vital, as stated in the field: "Every compound tells a story, and 2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetic acid is no exception."

Continued study and characterization of this compound could pave the way for groundbreaking advancements in medicinal applications.

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