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Solvent Yellow 72

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Identification
Molecular formula
C37H32O12
CAS number
34432-92-3
IUPAC name
[2-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate
State
State

At room temperature, this compound is typically in a solid state. It exists as crystalline powder and is insoluble in water but can dissolve in certain organic solvents.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.00
Boiling point (Celsius)
658.00
Boiling point (Kelvin)
931.00
General information
Molecular weight
676.65g/mol
Molar mass
676.6520g/mol
Density
1.2300g/cm3
Appearence

Solvent Yellow 72 typically appears as a yellow to orange crystalline powder.

Comment on solubility

Solubility of 2-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate (C37H32O12)

The solubility of complex organic compounds like 2-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate can be intricate, influenced by multiple factors. Here are several key points to consider:

  • Polarity: The structure contains various hydroxyl (–OH) and methoxy (–OCH3) groups, suggesting a degree of polarity that may enhance solubility in polar solvents.
  • Hydrophilicity vs Hydrophobicity: The presence of both hydrophilic (like –OH) and hydrophobic aromatic groups indicates that solubility could vary significantly in different solvents.
  • Solvent Effects: Solubility is expected to be greater in organic solvents due to the non-polar aromatic rings. It may be less soluble in water due to the bulk of the hydrophobic sections.
  • Temperature: Increased temperature might enhance solubility by overcoming intermolecular forces but can also depend on the specific solvent’s properties.

As a general behavior, one might say, "Like dissolves like", meaning that this compound is likely to be soluble in non-polar organic solvents while showing limited solubility in water. Understanding the unique balance of hydrophilicity and hydrophobicity in such complex structures is crucial for predicting their solubility behavior in various environments.

Interesting facts

Interesting Facts about 2-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate

This compound, with its complex structure, is a fascinating example of chemical innovation in organic synthesis. Here are some intriguing aspects of this remarkable molecule:

  • Biodiversity Connection: Many compounds like this one are often derived from natural sources and exhibit bioactive properties, making them valuable in pharmaceuticals and agrochemicals.
  • Functional Groups: The presence of multiple functional groups, such as hydroxyls and esters, enhances its reactivity and potential applications in various chemical reactions and syntheses.
  • Perylene Backbone: The compound features a perylene core, a popular choice in the field of organic electronics, known for its high charge mobility and photostability, useful for creating organic semiconductors.
  • Potential Applications: Due to its intricate design, this compound could find relevance in drug development, particularly in targeting diseases that involve oxidative stress or inflammation.
  • Research Interest: Ongoing research is likely to explore its antifungal, antibacterial, or anticancer properties, as various derivatives of similar structures have shown promising results in these fields.

As Dr. Marie Curie famously stated, "Nothing in life is to be feared, it is only to be understood." This compound is a testament to the strides we have made in understanding complex organic molecules. Each component in the structure serves a specific purpose, contributing to its potential utility in advancing science and technology.

In summary, the intricate nature of 2-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate not only underlines the beauty of chemical synthesis but also highlights the endless possibilities that exist in the realm of organic chemistry.

Synonyms
calphostin C
121263-19-2
CHEMBL261214
Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester, stereoisomer
Calphostin C from Cladosporium cladosporioides
924657-57-8
C44H38O14
1-[3,10-dihydroxy-12-(2-{[(4-hydroxyphenoxy)carbonyl]oxy}propyl)-2,6,7,11-tetramethoxy-4,9-dioxo-4,9-dihydroperylen-1-yl]propan-2-yl benzoate
CBiol_001843
KBioGR_000240
KBioSS_000240
1-[3,10-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-4,9-dioxoperylen-1-yl]propan-2-yl benzoate
SCHEMBL3469324
SCHEMBL13827621
KBio2_000240
KBio2_002808
KBio2_005376
KBio3_000479
KBio3_000480
LSUTUUOITDQYNO-UHFFFAOYSA-N
Bio1_000129
Bio1_000618
Bio1_001107
Bio2_000240
Bio2_000720
HMS1361L22
BDBM50500850
HB0160
MFCD00133155
AKOS024456712
IDI1_033990
(1R)-2-[12-[(2R)-2-(Benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethylcarbonic acid 4-hydroxyphenyl ester
DA-62014
HY-105416
CS-0025958
F82138
M04057
Calphostin C, Cladosporium cladosporioides - CAS 121263-19-2
Calphostin C from Cladosporium cladosporioides, >=90% (HPLC), powder
[2-[4,9-dihydroxy-12-[2-(4-hydroxyphenoxy)carbonyloxypropyl]-2,6,7,11-tetramethoxy-3,10-dioxo-perylen-1-yl]-1-methyl-ethyl] benzoate
1-(4,9-Dihydroxy-12-(2-(((4-hydroxyphenoxy)carbonyl)oxy)propyl)-2,6,7,11-tetramethoxy-3,10-dioxo-3,10-dihydroperylen-1-yl)propan-2-yl benzoate
1-(4,9-Dihydroxy-12-(2-(((4-hydroxyphenoxy)carbonyl)oxy)propyl)-2,6,7,11-tetramethoxy-3,10-dioxo-3,10-dihydroperylen-1-yl)propan-2-ylbenzoate
1-(4,9-dihydroxy-12-(2-((4-hydroxyphenoxy)carbonyloxy)propyl)-2,6,7,11-tetramethoxy-3,10-dioxo-3,10-dihydroperylen-1-yl)propan-2-yl benzoate
Benzoic acid 2-{4,9-dihydroxy-12-[2-(4-hydroxy-phenoxycarbonyloxy)-propyl]-2,6,7,11-tetramethoxy-3,10-dioxo-3,10-dihydro-perylen-1-yl}-1-methyl-ethyl ester
Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester,stereoisomer