CAS 59260-76-3
:(1R,2R)-2-aminocyclopentanol
Description:
(1R,2R)-2-aminocyclopentanol is a chiral amine characterized by its cyclopentane ring structure with an amino group and a hydroxyl group attached to the second carbon. This compound is notable for its stereochemistry, as the (1R,2R) designation indicates the specific three-dimensional arrangement of its atoms, which can significantly influence its chemical behavior and interactions. It is a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of both an amine and an alcohol functional group allows for hydrogen bonding, which can enhance its solubility in polar solvents. This compound is of interest in organic synthesis and pharmaceutical applications, particularly in the development of chiral drugs, due to its potential to act as a building block for more complex molecules. Additionally, its unique structure may impart specific biological activities, making it a subject of study in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C5H11NO
InChI:InChI=1/C5H11NO/c6-4-2-1-3-5(4)7/h4-5,7H,1-3,6H2/t4-,5-/m1/s1
SMILES:C1C[C@H]([C@@H](C1)O)N
Synonyms:- cyclopentanol, 2-amino-, (1R,2R)-
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Found 3 products.
Trans-2-amino-cyclopentanol
CAS:Formula:C5H11NOPurity:98%Color and Shape:LiquidMolecular weight:101.1469Trans-2-Amino-Cyclopentanol
CAS:<p>Trans-2-Amino-cyclopentanol is a chemical compound with the molecular formula CHCH(NH)COH. It is a colorless liquid that can be used as a solvent and as an intermediate in organic synthesis. Trans-2-Amino-cyclopentanol is found in human livers, where it may undergo biotransformations and acetylation. The isolated yield of this amine is dependent on the conditions of the reaction, such as temperature and pH. This amine has been shown to react chemically with anthracene to form trans-2-(aminomethyl)cyclohexanone, which can then be hydrolyzed by lipase to form trans-2-(aminomethyl)cyclohexanol. Trans-2-Amino-cyclopentanol is also used in chemoenzymatic reactions and can serve as an intermediate for the production of enantiopure pyrrolid</p>Formula:C10H22N2O2Purity:Min. 95%Molecular weight:202.29 g/mol



