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Usage

Chemical structure

A porphyrin molecule with three propionic acid side chains and an additional carboxyvinyl group attached to the porphyrin core.

Porphyrin family

Belongs to the class of organic compounds known as porphyrins, which are commonly found in living organisms.

Biological significance

Involved in various biological processes, including the transportation of oxygen and electron transfer.

Carboxyvinyl group

Contains a carboxylic acid functional group connected to a vinyl group, which contributes to its unique properties.

Functional groups

The presence of carboxylic acid and vinyl groups in the molecule.

Unique properties

The combination of porphyrin core, propionic acid side chains, and carboxyvinyl group gives the molecule distinct characteristics.

Potential applications

Due to its unique properties, the molecule has potential applications in fields such as medicine, catalysis, and materials science.

Molecular weight

Approximately 568.69 g/mol

Chemical stability

The molecule is stable under normal conditions, but may be sensitive to extreme pH levels or temperatures.

Solubility

The molecule is likely to be soluble in organic solvents such as chloroform, methanol, or dimethyl sulfoxide (DMSO).

Structural features

The molecule has a planar porphyrin core with four meso-carbon atoms, each connected to a methyl group, and three propionic acid side chains attached at the 2, 7, and 18 positions.

Synthesis

The molecule can be synthesized through various chemical reactions, such as condensation of pyrrole and aldehyde derivatives, followed by functionalization with propionic acid and carboxyvinyl groups.

Characterization

The molecule can be characterized using techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and elemental analysis.

Reactivity

The carboxylic acid and vinyl groups in the molecule may participate in various chemical reactions, such as esterification, amidation, or addition reactions.