| Identification | Back Directory | [Name]
trans-(1R,2R)-2-Aminocyclopentanol hydrochloride | [CAS]
31775-67-4 | [Synonyms]
(1R,2R)-2-Aminocyclopentano
(1R,2R)-2-amino-1-cyclopentanol
TRANS-(1R,2R)-2-AMINO-CYCLOPENTANOL HCL
trans-2-Aminocyclopentanol hydrochloride 97%
(1R,2R)-2-amino-1-cyclopentanol hydrochloride
rel-(1R,2R)-2-AMinocyclopentanol hydrochloride
(1R,2R)-rel-2-AMinocyclopentanol hydrochloride
rans-(1R,2R)-2-Aminocyclopentanolhydrochloride
trans-(1R,2R)-2-Aminocyclopentanol hydrochloride
(1R,2R)-2-Aminocyclopentanol Hydrochloride,99%e.e.
Cyclopentanol, 2-amino-, hydrochloride, (1R,2R)-rel-
trans-(1R,2R)-2-Aminocyclopentanol hydrochloride USP/EP/BP | [Molecular Formula]
C5H12ClNO | [MDL Number]
MFCD02683551 | [MOL File]
31775-67-4.mol | [Molecular Weight]
137.61 |
| Chemical Properties | Back Directory | [Melting point ]
191-196 °C(lit.)
| [storage temp. ]
Inert atmosphere,2-8°C | [InChI]
InChI=1/C5H11NO.ClH/c6-4-2-1-3-5(4)7;/h4-5,7H,1-3,6H2;1H/t4-,5-;/s3 | [InChIKey]
ZFSXKSSWYSZPGQ-TXRIQCMBNA-N | [SMILES]
N[C@@H]1CCC[C@H]1O.Cl |&1:1,5,r| |
| Hazard Information | Back Directory | [General Description]
trans-2-Aminocyclopentanol hydrochloride is an aminocyclanol. Its d,l-cis- and d,l-trans- forms have been synthesized. The trans-form of the product can be produced in large (multigram) scale via carbamate addition protocol. Cholinesterase inhibitory potential of cis-form of 2-aminocyclopentanol hydrochloride is higher (twofold) that of its trans-form. |
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