Chlorophyll c1

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Identification

Molecular formula
C35H32N4O10
CAS Number
11004-75-2
IUPAC Name
3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic acid
Molecular Weight
640.93g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1000g/cm3
Synonyms
Uroporphyrinogen III
Interesting facts

Interesting Facts about 3-[7,12,18-tris(2-carboxyethyl)-3,8,13,17-tetrakis(carboxymethyl)-5,10,15,20,21,22,23,24-octahydroporphyrin-2-yl]propanoic Acid

This compound, a highly intricate porphyrin derived structure, reveals a fascinating interplay of chemical architecture and biological significance. Porphyrins are known for their roles in essential biological functions, such as oxygen transport and photosynthesis, with hemoglobin and chlorophyll being prime examples.

Key Features

  • Complex Structure: The compound contains multiple carboxylic acid groups, which contribute to its solubility and reactivity in various environments.
  • Versatile Applications: Given its porphyrin framework, this compound could be explored for applications in fields such as photodynamic therapy, sensors, and catalysis.
  • Metal Coordination: Porphyrins often exhibit the ability to chelate metal ions, potentially allowing them to participate actively in electron transfer reactions.

The structure’s intricate design, specifically the presence of multiple carboxyethyl and carboxymethyl groups, enhances its potential to interact with biomolecules. This complex nature necessitates thorough research to unlock its possible therapeutic applications. As noted by prominent chemists, "The modification of porphyrins can lead to innovative solutions in drug design and delivery."

Overall, this compound stands as a testament to the creativity found within chemical synthesis and how intricate design can lead to exciting possibilities in both scientific research and practical applications.

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