250230-51-4

Basic information

• Product Name: 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-
• Synonyms: 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-;1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-23H,25H-Benzo[b]porphine-9,13-dipropanoic acid
• CAS NO: 250230-51-4
• Molecular Formula: C40H42N4O9
• Molecular Weight: 722.791
• Mol File: 250230-51-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-(250230-51-4)
• EPA Substance Registry System: 23H,25H-Benzo[b]porphine-9,13-dipropanoic acid, 1,22a-dihydro-19-(1-hydroxyethyl)-1,2-bis(methoxycarbonyl)-8,14,18,22a-tetramethyl-(250230-51-4)

Safety Data

• Hazardous Substances Data: 250230-51-4(Hazardous Substances Data)

Usage

Porphyrin Structure

A heterocyclic macrocyclic compound.
Consists of four pyrrole rings connected by methine bridges.

Functional Groups

Two Propionic Acid Groups: Provide acidity and can participate in chemical reactions.
Two Methoxycarbonyl Groups: Responsible for the carbonyl group attached to an oxygen and a methoxy group; can participate in esterification reactions.
One Hydroxyethyl Group: Contains an alcohol (-OH) group bonded to an ethyl group (-CH2-CH2-OH); can participate in hydrogen bonding and other reactions involving alcohols.

Derivative of Porphine

Porphine is a parent compound for various porphyrin derivatives.
Derivatives often possess altered properties compared to the parent compound.

Applications

Chemistry and Biochemistry:
Used in the study of porphyrin derivatives.
Investigated for potential applications in various fields such as medicine, materials science, and catalysis.
May have applications in photodynamic therapy due to the photophysical properties of porphyrins.
Can serve as a model compound for studying structure-activity relationships in porphyrin chemistry.
Potential use in sensing and detection due to the sensitivity of porphyrins to their environment.

Potential Properties

Photophysical Properties: Ability to absorb and emit light, which can be utilized in various applications including sensors and imaging.
Chemical Reactivity: Interaction with other molecules, including potential for coordination chemistry with metal ions.
Solubility: Depending on the specific groups attached, solubility in different solvents may vary, impacting its applications and handling.
Stability: Stability under various conditions such as light, temperature, and pH, important for practical applications.

Significance

Understanding the properties and reactivity of this compound contributes to the broader field of porphyrin chemistry and its applications in diverse fields.