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Mitomycin C

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Identification
Molecular formula
C15H18N4O5
CAS number
50-07-7
IUPAC name
2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione
State
State

Mitomycin C is typically a solid at room temperature. It is stable in this form and often handled as a powder for dissolution prior to use in medical or research settings.

Melting point (Celsius)
226.00
Melting point (Kelvin)
499.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
334.33g/mol
Molar mass
334.3250g/mol
Density
1.3000g/cm3
Appearence

Mitomycin C appears as a blue-violet crystalline solid, often used in its powder form for medical and laboratory applications. The compound commonly crystallizes in various forms depending on solvent and crystallization conditions, making its appearance variable under different circumstances.

Comment on solubility

Solubility of 2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione

The solubility characteristics of 2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione can be quite intriguing. This compound, which is a derivative of tetrahydronaphthalene-1,4-dione, exhibits particular solubility behavior that can be influenced by various factors:

  • Polarity: The presence of the aziridinyl moiety contributes to the overall polarity of the compound, influencing its solubility in polar solvents.
  • Solvent Interaction: This compound is commonly soluble in polar organic solvents such as methanol and ethanol, but may have limited solubility in non-polar solvents like hexane.
  • Temperature Effects: Like many organic compounds, the solubility of this substance may increase with temperature, allowing for better dissolution in solvents.

Due to its unique structure, understanding the solubility of 2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione is essential for applications in fields like pharmaceuticals and materials science. It can be said that “like dissolves like,” and thus, the choice of solvent plays a critical role in achieving the desired solubility for experimental or practical applications.

In summary, factors such as polarity, solvent choice, and temperature can significantly impact the solubility of this compound, making it a versatile entity in various chemical contexts.

Interesting facts

Interesting Facts About 2-(Aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione

The compound 2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione is a fascinating example of a bicyclic compound, showcasing both structural complexity and potential biological significance.

Structural Highlights

  • Bicyclic Nature: The compound contains a naphthalene core, which is a fused bicyclic structure, making it an intriguing subject for study in organic chemistry.
  • Aziridine Ring: The presence of the aziridinyl group adds unique reactivity and properties due to its three-membered ring structure, which is known for its strain and susceptibility to undergo ring-opening reactions.

Potential Applications

  • Biomedical Research: Compounds with such structures often exhibit interesting biological activities, making them potential candidates for drug development.
  • Synthetic Chemistry: The unique reactivity of the aziridine ring can be exploited in various synthesis pathways, enabling chemists to create more complex molecules.

In the field of medicinal chemistry, there is a growing interest in compounds that contain naphthalene and derivatives due to their role in numerous natural products and synthetic pharmaceuticals. Researchers are particularly focused on exploring their mechanisms of action and therapeutic potential. This compound serves as a reminder of the intricate connections between chemical structure and biological function. As one scholar aptly noted, “The beauty of chemistry lies in its ability to bridge the gap between structure and function, providing insight into life’s molecular tapestry.”

Conclusion

2-(aziridin-1-yl)-5,6,7,8-tetrahydronaphthalene-1,4-dione exemplifies how even complex compounds can inspire further research and discovery. Its unique features not only challenge chemists but also pave the way for advancements in various scientific fields.

Synonyms
443-76-5
BRN 0184025
2-(1-Aziridinyl)-5,6,7,8-tetrahydro-1,4-naphthalenedione
2-Ethylenimino-5,6,7,8-tetrahydronaphthoquinone-1,4
A 137
A-137
2-ethyleneimino-5,6,7,8-tetrahydronaphthoquinone
2-Ethyleneimino-5,6,7,8-tetrahydronaphthoquinone-1,4
2-(1-Azridinyl)-5,6,7,8-tetrahydro-1,4-naphthalenedione
2-Aethylenimino-5.6.7.8-tetrahydro-naphthochinon-1 4 [German]
DTXSID50196109
4-20-00-00013 (Beilstein Handbook Reference)
2-Aethylenimino-5.6.7.8-tetrahydro-naphthochinon-1 4
1,4-Naphthalenedione, 2-(1-aziridinyl)-5,6,7,8-tetrahydro-
1,4-NAPHTHOQUINONE, 2-(1-AZIRIDINYL)-5,6,7,8-TETRAHYDRO-
SCHEMBL3270925
DTXCID10118600
MWOHJANRPKUELV-UHFFFAOYSA-N
1,4-Naphthalenedione, 2-(1-aziridinyl)-5,6,7,8-tetrahydro-(9CI)