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Gossypol

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Identification
Molecular formula
C30H30O8
CAS number
303-45-7
IUPAC name
5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol
State
State

At room temperature, gossypol is solid. Typically found as crystalline yellow powder.

Melting point (Celsius)
176.00
Melting point (Kelvin)
449.15
Boiling point (Celsius)
863.00
Boiling point (Kelvin)
1 136.15
General information
Molecular weight
518.55g/mol
Molar mass
518.5500g/mol
Density
1.3550g/cm3
Appearence

Gossypol appears as a yellow to yellow-brown crystalline solid, often presented in powder form.

Comment on solubility

Solubility of 5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol

The solubility of the compound 5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol (C30H30O8) can be influenced by several factors, primarily due to its complex structure which incorporates multiple hydroxyl (-OH) groups. The presence of these functional groups generally enhances solubility in polar solvents like water.

  • Water Solubility: Compounds with multiple hydroxyl groups tend to be more soluble in water, owing to their ability to form hydrogen bonds.
  • Organic Solvent Solubility: In non-polar solvents, solubility may decrease due to the hydrophobic nature of certain parts of the molecule. Ethanol and methanol may provide a favorable environment due to their polar characteristics.
  • Temperature Effects: Solubility can vary with temperature. Generally, an increase in temperature enhances solubility for many organic compounds.

In summary, while the indicated structure suggests potential solubility in polar solvents due to the hydroxyl groups, the overall solubility behavior of this compound would require empirical investigation for a complete understanding. As with many organic compounds, the interaction between molecular structure and solvent properties is fundamental in determining solubility.

Interesting facts

Interesting Facts about 5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol

This fascinating compound belongs to a class of organic molecules characterized by their complex structure and potential biological activities. Here are some notable points:

  • Multi-Hydroxyl Functionality: The presence of multiple hydroxyl (–OH) groups in its structure suggests potential antioxidant properties. Compounds rich in hydroxyl groups are often explored for their ability to scavenge free radicals.
  • Phenolic Compounds: As a phenolic compound, it may exhibit unique chemical behaviors, including strong interactions with other molecules, making it valuable in various applications, from pharmaceuticals to materials science.
  • Medicinal Potential: Structures similar to this compound have been studied for their anticancer, anti-inflammatory, and antimicrobial properties. The specific arrangement of substituents on the benzene ring may play a significant role in these biological activities.
  • Synthetic Interest: The synthesis of such complex compounds often requires advanced synthetic techniques, including multi-step reactions and protecting group strategies, making it a topic of interest in the field of synthetic organic chemistry.
  • Naturally Occurring Precursors: Many compounds with similar structural motifs can be found in natural sources, such as plants, where they may serve as defense mechanisms against pests or pathogens.

In conclusion, 5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol represents a remarkable intersection of chemistry and biology, showcasing the intricate relationship between molecular structure and function. As scientists continue to explore this compound, it may lead to valuable discoveries in various fields of research.

Synonyms
hbdde
154675-18-0
Hhbpdde
2,2',3,3',4,4'-Hexahydroxy-1,1'-biphenyl-6,6'-dimethanol dimethyl ether
5-(methoxymethyl)-4-[2,3,4-trihydroxy-6-(methoxymethyl)phenyl]benzene-1,2,3-triol
CHEMBL59451
[1,1'-Biphenyl]-2,2',3,3',4,4'-hexol,6,6'-bis(methoxymethyl)-
CHEMBL437222
CHEMBL537897
BiomolKI_000067
BiomolKI2_000071
BMK1-G7
BSPBio_001115
KBioGR_000455
KBioSS_000455
SCHEMBL1272421
CHEBI:94660
KBio2_000455
KBio2_003023
KBio2_005591
KBio3_000849
KBio3_000850
DTXSID20935042
Bio2_000388
Bio2_000868
HMS1362G17
HMS1792G17
HMS1990G17
HMS3403G17
BDBM50043774
BDBM50375658
BDBM50375660
AKOS030533055
CCG-100671
IDI1_002143
NCGC00163390-01
NCGC00163390-02
NCGC00163390-03
NCGC00163390-04
DA-74021
TS-08917
HY-131305
CS-0132740
HBDDE - CAS 154675-18-0
BRD-K56064827-001-03-9
BRD-K56064827-001-04-7
Q27166474
6,6''-Bis-methoxymethyl-biphenyl-2,3,4,2'',3'',4''-hexaol
6,6'-Bis(methoxymethyl)[1,1'-biphenyl]-2,2',3,3',4,4'-hexol