Interesting facts
Interesting Facts about (1S,2R)-2-phenylcyclopropanamine
(1S,2R)-2-phenylcyclopropanamine, a compound belonging to the class of cyclopropane derivatives, has drawn attention due to its intriguing structural features and potential pharmacological applications. Here are some captivating insights:
- Structural Attractiveness: The cyclopropane ring in (1S,2R)-2-phenylcyclopropanamine introduces unique strain characteristics, which can impact the reactivity and interactions of the compound in biological systems.
- Chirality Matters: The (1S,2R) configuration of this compound marks it as a chiral molecule. Chirality plays a critical role in drug development since the two enantiomers can exhibit vastly different biological activities.
- Potential Therapeutic Uses: Studies suggest that compounds related to (1S,2R)-2-phenylcyclopropanamine may possess interesting pharmacological properties. These include potential uses in treating disorders related to the central nervous system.
- Synthetic Challenges: The synthesis of (1S,2R)-2-phenylcyclopropanamine often involves intricate steps, highlighting the challenges associated with creating cyclopropane-containing compounds in laboratory settings. Techniques such as stereoselective synthesis and asymmetric synthesis are typically employed.
- Foundation for Further Research: The unique properties of (1S,2R)-2-phenylcyclopropanamine create a platform for further exploration. Researchers are continually investigating derivatives and modifications to harness the compound's potential.
In summary, (1S,2R)-2-phenylcyclopropanamine is not just a simple organic compound; it epitomizes the complex interplay between structure, function, and biological activity. As a chemist or a student delving into organic chemistry, understanding such compounds can pave the way to discoveries that impact drug design and development.
Synonyms
(1S,2R)-2-phenylcyclopropanamine
(+)-Tranylcypromine
DTXSID801315454
trans-2-phenylcyclopropanamine
DTXCID801745360
988-714-7
3721-28-6
(1S,2R)-2-phenylcyclopropan-1-amine
trans-2-Phenylcyclopropylamine
(-)-Tranylcypromine
(1S,2R)-2-Phenyl-cyclopropylamine
(1S,2R)-tranylcypromine
CHEMBL257990
(1s,2r)-2-phenylcyclopropylamine
MFCD01735853
Cyclopropanamine, 2-phenyl-, (1S,2R)-
l-Tranylcypromine
2-Phenyl-1-aminocyclopropane, trans-
Cyclopropylamine, 2-phenyl-, (1S-trans)-
trans-2-phenylcyclopropan-1-amine
trans-(-)-2-Phenylcyclopropanamine
1tnl
(1S,2R)-2-phenyl-1-cyclopropanamine
MLS001306494
SCHEMBL145650
(1R)-2-Phenylcyclopropanamine
orb2277566
(1S,2R)-trans-tranylcypromine
CHEBI:94791
BRD9146
CHEBI:131511
HMS2089B04
(+)-trans-2-Phenylcyclopropylamine
BRD-9146
(1S-trans)-2-Phenylcyclopropanamine
BDBM50236898
STL563237
(+)-trans-2-Phenyl-cyclopropyl-amin
1s,2r-trans-2-phenylcyclopropylamine
AKOS027327308
(1S,2R)-(+)-2-phenylcyclopropylamine
NCGC00179670-01
AS-81089
SMR000039637
Cyclopropanamine, 2-phenyl-, trans-(+)-
CYCLOPROPYLAMINE, 2-PHENYL-, trans-
DB-234630
CS-0094394
NS00068412
EN300-222059
AN-584/40205785
BRD-K88809146-003-02-1
BRD-K88809146-003-04-7
Solubility of (1S,2R)-2-phenylcyclopropanamine
(1S,2R)-2-phenylcyclopropanamine is an intriguing compound, and its solubility characteristics provide valuable insights into its behavior in various environments. Understanding its solubility can be approached through several key factors:
It's essential to note that while empirical data on the solubility of (1S,2R)-2-phenylcyclopropanamine may be limited, its structure suggests a balanced amphiphilicity, which can lead to moderate solubility in various organic solvents. As with many chemical compounds, conducting solubility tests under controlled conditions will provide a clearer picture of its behavior in practical applications.
In summary, the solubility of (1S,2R)-2-phenylcyclopropanamine is governed by its molecular structure and the properties of the solvent used, making it a captivating subject for further exploration in chemical assessments.