| Identification | More | [Name]
(3R)-(-)-3-Aminopyrrolidine dihydrochloride | [CAS]
116183-81-4 | [Synonyms]
3-PYRROLIDINAMINE, DIHYDROCHLORIDE, (3R)-
(3R)-(-)-3-AMINOPYRROLIDINE DIHYDROCHLORIDE
PYRROLIDIN-3-YL-AMINE, (R), DIHYDROCHLORIDE
(R)-(-)-3-AMINOPYRROLIDINE DIHYDROCHLORIDE
(R)-3-AMINOPYRROLIDINE DIHYDROCHLORIDE
(R)-PYRROLIDIN-3-AMINE DIHYDROCHLORIDE
(R)-PYRROLIDIN-3-YLAMINE DIHYDROCHLORIDE
(R)-(-)-3-AMINOPYRROLIDINE 2HCL
3-Aminopyrrolidine dihvdrochlon
(3R)-(-)-3-Aminopyrrolidine2HCl
(R)-(-)-3-AMINOPYRROLIDINE DIHYDROCHLORIDE,98% | [EINECS(EC#)]
634-214-6 | [Molecular Formula]
C4H12Cl2N2 | [MDL Number]
MFCD00070604 | [Molecular Weight]
159.06 | [MOL File]
116183-81-4.mol |
| Chemical Properties | Back Directory | [Melting point ]
283°C (dec.) | [refractive index ]
-1.1 ° (C=10, H2O) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
Powder | [color ]
White to off-white | [optical activity]
[α]20/D 1.8°, c = 1 in H2O | [Water Solubility ]
very faint turbidity | [Sensitive ]
Hygroscopic | [Detection Methods]
T | [BRN ]
5852700 | [InChIKey]
NJPNCMOUEXEGBL-RZFWHQLPSA-N | [CAS DataBase Reference]
116183-81-4(CAS DataBase Reference) | [Storage Precautions]
Air sensitive |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3 | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
(R)-3-Aminopyrrolidine dihydrochloride is an optically active 3-aminopyrrolidine derivative, which can be used as a key intermediate in the synthesis of chiral drugs or pesticides. | [Uses]
(R)-3-Aminopyrrolidine dihydrochloride is a key intermediate in the synthesis of chiral drugs or pesticides, and it can be used in the synthesis of vinylpyrrolidone-Cephaloridine drugs. | [Synthesis]
(3R)-(-)-3-Aminopyrrolidine dihydrochloride was prepared by reacting (R)-3-(tert-butoxycarbonyl-amino)-pyrrolidine in methanol with chloroform Sulfone at room temperature for 6-9 hours. |
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