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2-Adamantanamine

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Identification
Molecular formula
C10H17N
CAS number
702-99-4
IUPAC name
adamantan-2-amine
State
State

At room temperature, 2-Adamantanamine is a solid. Its robust adamantane structure contributes to its stability and solid-state form at ambient conditions.

Melting point (Celsius)
257.00
Melting point (Kelvin)
530.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
151.24g/mol
Molar mass
151.2420g/mol
Density
1.0876g/cm3
Appearence

2-Adamantanamine appears as a white crystalline powder. It is solid in form and has a distinctive appearance due to its adamantane structure, which gives it a three-dimensional diamond-like framework.

Comment on solubility

Solubility of Adamantan-2-amine

Adamantan-2-amine (C10H17N) exhibits interesting solubility characteristics that can be influenced by several factors. Generally speaking, this compound is categorized as a moderately soluble organic amine in polar solvents.

Factors Affecting Solubility

The solubility of adamantan-2-amine can be impacted by:

  • Temperature: Increased temperatures typically enhance solubility in many solvents.
  • pH Levels: The behavior of amines in acidic or basic environments can lead to varying solubility; for instance, in acidic solutions, it tends to form salts which are more soluble.
  • Presence of Other Solvents: The addition of certain solvents can result in improved solubility due to synergistic effects.

General Solubility Profile

In general:

  • Water solubility: Adamantan-2-amine is somewhat soluble in water due to its amine group which can participate in hydrogen bonding.
  • Solubility in organic solvents: It is typically more soluble in organic solvents like ethanol and dimethyl sulfoxide (DMSO).

To summarize, while adamantan-2-amine does exhibit moderate solubility, one must consider specific conditions such as temperature, pH, and solvent type to ensure optimal dissolution. As always, "solubility is key to understanding the behavior and application of chemical compounds."

Interesting facts

Interesting Facts about Adamantan-2-amine

Adamantan-2-amine, a fascinating compound within the realm of organic chemistry, is a member of the amine class due to the presence of an amino group (-NH2). It is derived from adamantane, which is known for its unique cage-like structure composed of fused cycloalkane rings. This molecular architecture gives adamantan-2-amine a variety of interesting properties and potential applications.

Key Highlights:

  • Structural Uniqueness: The adamantane core provides a three-dimensional framework that is both rigid and stable, making it an ideal starting point for synthesizing various derivatives.
  • Biological Significance: Compounds with similar structures have been studied for their potential as pharmaceuticals, particularly in antiviral and anticancer research.
  • Interactions with Biological Systems: The aminated version may exhibit intriguing interactions within biological membranes, potentially leading to novel applications in drug delivery systems.
  • Versatile Synthesis: Adamantan-2-amine can be synthesized through various methods, allowing for the incorporation of different functional groups, which can tailor its properties for specific uses.

As noted by many researchers, “the unique three-dimensional structure of adamantan derivatives allows them to engage in unexpected chemical reactions,” emphasizing the compound's versatility. Adamantan-2-amine’s potential in scientific research is boundless, paving the way for exploratory paths in medicinal chemistry and materials science. This compound is certainly worth further study for anyone interested in the cutting-edge applications of organic chemistry!

Synonyms
2-aminoadamantane
13074-39-0
2-Adamantanamine
2-Adamantylamine
Tricyclo[3.3.1.13,7]decan-2-amine
JP 60
NSC 127842
Tricyclo(3.3.1.1(3,7))decan-2-amine
DTXSID90156707
Tricyclo(3.3.1.13,7)decan-2-amine
2-Adamantanamine (8CI)
DTXCID4079198
Tricyclo(3.3.1.13,7)decan-2-amine (9CI)
qzwnxxinfabalm-uhfffaoysa-n
adamantan-2-amine
adamantan-2-ylamine
MFCD00078225
CHEMBL1170792
adamantane-2-ylamine
NSC-127842
F1928-0024
2-amino-adamantane
tricyclo[3.3.1.1~3,7~]decan-2-amine
NSJ4EPG7F7
Oprea1_605085
SCHEMBL75970
SCHEMBL991773
AC17
SCHEMBL1714862
SCHEMBL2400612
SCHEMBL4657616
SCHEMBL4688717
SCHEMBL12876277
SCHEMBL17203865
SCHEMBL27820570
HMS1787I03
SMSSF-0044387
ALBB-013876
NAA07439
BDBM50482329
NSC127842
SBB002575
STK099532
AKOS000113996
AKOS001033453
AKOS016037117
LS-13853
PD096138
ST091025
SY180443
DB-003066
CS-0094367
EN300-57378
D94469