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Naphthazarin

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Identification
Molecular formula
C14H8O4
CAS number
475-38-7
IUPAC name
2,5-dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone
State
State

At room temperature, Naphthazarin is typically in solid form. It is neither soluble in water nor other polar solvents, limiting its state under standard conditions to solid powders or crystals. It may require specific conditions to dissolve or become part of a solution.

Melting point (Celsius)
196.00
Melting point (Kelvin)
469.15
Boiling point (Celsius)
546.00
Boiling point (Kelvin)
819.15
General information
Molecular weight
290.28g/mol
Molar mass
290.2830g/mol
Density
1.3000g/cm3
Appearence

Naphthazarin typically appears as a crystalline solid. It is often characterized by its bright color, which can range from deep reds to purples. The compound is fairly stable under normal conditions but may be sensitive to heat and light exposure, potentially altering its color and composition.

Comment on solubility

Solubility of 2,5-Dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone (C14H8O4)

Understanding the solubility of 2,5-dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone is key to grasping its potential applications and interactions in various solvents. This compound is characterized by a complex structure that can influence its solubility in different environments. Here are some important points regarding its solubility:

  • Polar vs. Nonpolar Solvents: Compounds with hydroxyl groups, like this one, typically exhibit greater solubility in polar solvents, including water and alcohols. This is due to hydrogen bonding capabilities.
  • Influence of Substituents: The presence of multiple aromatic rings and functional groups can complicate solubility. The substituents can either hinder or enhance solubility based on their nature and spatial arrangement.
  • Saturation Levels: The solubility can also depend on the temperature and concentration, where increasing temperature often leads to improved solubility due to enhanced molecular motion.

In conclusion, while C14H8O4 may show distinct solubility trends in various solvents, thorough experimentation and analysis are required to pinpoint its solubility characteristics accurately. As always, the **interaction** of molecular structure and solvent nature plays a critical role in determining solubility behavior.

Interesting facts

Interesting Facts about 2,5-Dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone

The compound known as 2,5-dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone is a fascinating member of the family of quinones, known for their versatility and utility in various chemical and biological contexts. Here are some engaging points about this compound:

  • Biological Importance: Compounds like this benzoquinone can exhibit significant biological activities, making them potential candidates for pharmaceutical research. They may play roles in antioxidant activity, antibacterial tendencies, or even in anti-cancer properties.
  • Structural Complexity: The structure of this compound showcases an intricate arrangement that connects the indole units through a benzoquinone core. This complex configuration often results in unique chemical reactivity and properties.
  • Natural Sources: Many benzoquinones and their derivatives are found in nature, particularly in plants. This compound could be involved in the plant's defense mechanisms against herbivores or pathogens.
  • Synthesis Potential: The methodology for synthesizing such complex organic compounds often involves multi-step synthetic routes that are a testament to the creativity and ingenuity of chemists. Understanding these synthetic pathways can open avenues for the development of new materials or drugs.

In summary, the study of 2,5-dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]-1,4-benzoquinone can provide insights into not only advanced organic chemistry but also its application in biological systems. As the fields of medicinal chemistry and biochemistrycontinue to expand, the significance of such compounds will undoubtedly grow.

Synonyms
Cochliodinol
11051-88-0
2,5-dihydroxy-3,6-bis[5-(3-methylbut-2-enyl)-1H-indol-3-yl]cyclohexa-2,5-diene-1,4-dione
BRN 5188623
Cochliodinol,fromChaetomiumglobosum.
DTXSID20149268
3,6-Bis(5-(3-methyl-2-butenyl)indol-3-yl)-2,5-dihydroxy-p-benzoquinone
5-25-03-00406 (Beilstein Handbook Reference)
NSC695240
2,5-Cyclohexadiene-1,4-dione, 2,5-dihydroxy-3,6-bis(5-(3-methyl-2-butenyl)-1H-indol-3-yl)-
p-Benzoquinone, 3,6-bis(5-(3-methyl-2-butenyl)indol-3-yl)-2,5-dihydroxy-
2,5-Dihydroxy-3,6-bis(5-(3-methyl-2-butenyl)-1H-indol-3-yl)-2,5-cyclohexadiene-1,4-dione
2,5-dihydroxy-3,6-bis(5-(3-methylbut-2-enyl)-1H-indol-3-yl)cyclohexa-2,5-diene-1,4-dione
Cochliodinol o Isocochliodinol
DTXCID5071759
BCP16319
BS-1115
HY-W714006
NSC-695240
DA-62435
CS-0820298
F86505
2,5-Cyclohexadiene-1,4-dione, 2,5-dihydroxy-3,6-bis[5-(3-methyl-2-butenyl)-1H-indol-3-yl]; 2,5-Dihydroxy-3,6-bis[5-(3-methyl-2-buten-1-yl)-1H-indol-3-yl]-2,5-cyclohexadiene-1,4-dione; Cochliodinol; NSC 695240