Skip to main content

Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate

ADVERTISEMENT
Identification
Molecular formula
C7H13N3O2
CAS number
104188-49-4
IUPAC name
methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate
State
State

At room temperature, Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate is in a solid state. It remains stable under standard conditions and does not readily evaporate or transition into other states without specific chemical reactions or thermal input. Handling should ensure it is kept dry to prevent decomposition or reaction with moisture.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
169.20g/mol
Molar mass
169.1490g/mol
Density
1.1800g/cm3
Appearence

Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate is typically a light yellow to off-white crystalline powder. It has a somewhat granular appearance and may form clusters or agglomerates in its solid state. It is usually stored in a cool, dry place to maintain its physical stability and integrity. Protective measures should be taken to avoid moisture as it can affect its purity and functionality.

Comment on solubility

Solubility of Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate

The solubility of methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate can be influenced by multiple factors. Generally speaking, compounds with polar functional groups tend to exhibit increased solubility in polar solvents like water, while non-polar regions interact better with non-polar solvents.

In this case:

  • Functional Groups: The presence of amino (-NH2) and carboxylate (-COO) groups suggests that this compound may be soluble in polar solvents.
  • Cyclic Structure: The tetrahydro-diazepine ring may enhance overall solubility by providing a flexible and polarizable structure.
  • pH Sensitivity: Solubility can also vary with pH; the carboxylate group can exist in different protonation states depending on the pH, affecting solubility.

As a result, we might find that methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate is more soluble in polar solvents compared to non-polar solvents, making it suitable for use in various chemical applications that require solubility in aqueous environments.

Interesting facts

Interesting Facts about Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate

Methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate is a fascinating member of the diazepine family and holds significant interest in both chemical research and pharmacology. Here are some intriguing aspects of this compound:

  • Structural Complexity: This compound features a unique bicyclic structure, combining a diazepine ring with a carboxylate side group. This intricate architecture contributes to its diverse biological activities.
  • Pharmacological Potential: Molecules similar to this one have been studied for their effects on the central nervous system. Due to the presence of the diazepine core, it may exhibit properties that could be leveraged in developing anxiolytic (anti-anxiety) medications.
  • Research Applications: This compound and its derivatives are of particular interest in medicinal chemistry. Researchers actively explore its potential as a template for novel drugs, especially within the realm of neuropharmacology.
  • Synthetic Routes: Its synthesis often involves innovative organic reactions, making it a subject of interest for students and chemists looking to deepen their understanding of organic synthesis and reaction mechanisms.
  • Interdisciplinary Connections: The study of this compound bridges various fields, including organic chemistry, pharmacology, and medicinal chemistry, emphasizing the interconnected nature of scientific disciplines.

In summary, methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate serves as an excellent example of how modern chemistry can lead to the discovery of promising therapeutic agents. Its structural and pharmacological characteristics highlight the endless possibilities within the realm of chemical compounds.

Synonyms
26281-63-0
methyl 2-amino-4,5,6,7-tetrahydro-1H-1,3-diazepine-7-carboxylate
SCHEMBL29642421
DTXSID60275050