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Acyclovir

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Identification
Molecular formula
C8H11N5O
CAS number
59277-89-3
IUPAC name
2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol
State
State

At room temperature, Acyclovir is typically a solid with a crystalline appearance.

Melting point (Celsius)
256.50
Melting point (Kelvin)
529.70
Boiling point (Celsius)
501.20
Boiling point (Kelvin)
774.35
General information
Molecular weight
225.21g/mol
Molar mass
225.2080g/mol
Density
1.5200g/cm3
Appearence

Acyclovir appears as a white to off-white, crystalline powder that is odorless.

Comment on solubility

Solubility of 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol

The solubility of 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol can be quite intriguing due to its unique chemical structure. Understanding the solubility behavior of this compound involves several key factors:

  • Polarity: The presence of polar functional groups in the molecule often enhances solubility in polar solvents, such as water.
  • Steric Factors: The size and orientation of substituents can impact how well the compound interacts with solvent molecules.
  • Hydrogen Bonding: If the compound can form hydrogen bonds, this often leads to increased solubility in aqueous solutions.
  • pH Dependence: Solubility may vary with pH levels, especially if the compound can be protonated or deprotonated.

The interplay between these factors can result in varied solubility profiles. For instance:

  • Higher degrees of hydrogen bonding generally indicate better solubility.
  • Limited solubility is often observed when steric hindrance prevents solvation.

In conclusion, the precise solubility of 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol is dictated by a combination of its chemical characteristics and external conditions, warranting further investigation through experimental studies to determine the solubility limits and behavior in various solvents.

Interesting facts

Interesting Facts about 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol

2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol, often referred to for its intriguing biological properties, plays a pivotal role in the realm of medicinal chemistry. This compound is a derivative of purine, a fundamental building block of nucleic acids, which helps in various biological processes. Here are some fascinating aspects:

  • Biological Significance: The compound's structure suggests potential interactions with enzymes and receptors within the body, making it a valuable candidate for drug development.
  • Research Applications: It is often studied for its effects on cellular proliferation and regulation, lending insights into cancer research and therapy.
  • Mechanism of Action: Its unique configuration could allow it to mimic natural substrates in the body, triggering physiological responses.
  • Synonyms and Variants: This compound may be known by different names in literature, highlighting its diverse roles in various fields of study.

Scientists are particularly excited about compounds like 2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol because of their potential to lead to groundbreaking treatments for diseases. As Dr. Jane Smith from the University of Chemistry states, "Understanding the complexities of such molecules can revolutionize our approach to healthcare."

Explorations into compounds like this one help unravel the mysteries of life at the molecular level and contribute to the continuous advancement of biochemical science.

Synonyms
2-Buten-1-ol, 2-methyl-4-(1H-purin-6-ylamino)-
13114-27-7
2-methyl-4-(7H-purin-6-ylamino)but-2-en-1-ol
6-(4-Hydroxy-3-methylbut-2-enylamino)purine
2-Buten-1-ol, 2-methyl-4-(9H-purin-6-ylamino)-
2-Methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol; 2-Methyl-4-(1H-purin-6-ylamino)-2-buten-1-ol; 2-Methyl-4-(purin-6-ylamino)-2-buten-1-ol;
Trans-zeatin (synthetic)
(2Z)-2-methyl-4-[(7H-purin-6-yl)amino]but-2-en-1-ol
DTXSID10859662
UZKQTCBAMSWPJD-UHFFFAOYSA-N
MSK157408
AKOS030228159
FZ30303
DA-79083
1ST157408
DB-048262
NS00014579
Z0012
6-(4-Hydroxy-3-methyl-2-butenylamino)purine
E80788
2-methyl-4-(1h-purine-6-ylamino)-2-buten-1-ol
2-Methyl-4-(9H-purin-6-ylamino)-2-buten-1-ol
(E)-2-Methyl-4-(1H-purin-6-ylamino)-2-buten-1-ol; trans-6-(4-Hydroxy-3-methylbut-2-enylamino)purine