ChemicalBook--->CAS DataBase List--->68327-11-7

68327-11-7

68327-11-7 Structure

68327-11-7 Structure
IdentificationMore
[Name]

trans-2-Aminocyclopentanol hydrochloride
[CAS]

68327-11-7
[Synonyms]

TRANS-(1R,2R)-2-AMINO-CYCLOPENTANOL HCL
TRANS-(-)-2-AMINOCYCLOPENTANOL HYDROCHLORIDE
TRANS-2-AMINOCYCLOPENTANOL HYDROCHLORIDE
Trans-(-)-2-aminocyclopentanolHCl
(1R,2R)-2-AMINOCYCLOPENTANOL HYDROCHLORIDE
[1R,2R]-trans-2-Aminocyclopentanol hydrochloride
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C5H12ClNO
[MDL Number]

MFCD02683551
[Molecular Weight]

137.61
[MOL File]

68327-11-7.mol
Chemical PropertiesBack Directory
[Melting point ]

191-196 °C(lit.)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder to crystal
[color ]

White to Light yellow to Light orange
[BRN ]

4143621
[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]

[C@@H]1(O)CCC[C@H]1N.[H]Cl |&1:0,5,r|
[CAS DataBase Reference]

68327-11-7(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

(1R,2R)-2-Aminocyclopentanol hydrochloride is a useful research chemical.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H302-H319
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
[WGK Germany ]

3
[HS Code ]

29221990
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

trans-2-Aminocyclopentanol hydrochloride(68327-11-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

68327-11-7(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

Carbamic acid, N-[(1R,2R)-2-hydroxycyclopentyl]-, phenylmethyl ester

672310-36-0

trans-2-Aminocyclopentanol hydrochloride

68327-11-7

To a 100 mL autoclave was added 15 g (70.7 mmol) of (R,R)-2-benzyloxycarbonylaminocyclopentanol and 0.3 g of 5% palladium-carbon catalyst, and 45 mL of degassed methanol under nitrogen protection. The reaction mixture was stirred under 2 MPa hydrogen pressure at 50 °C for 3 hours. Upon completion of the reaction, the palladium-carbon catalyst was removed by diatomaceous earth filtration. Concentrated hydrochloric acid was slowly added to the filtrate to adjust the pH to 3. Subsequently, the aqueous phase was concentrated to afford 7.9 g of trans-(-)-2-aminocyclopentanol hydrochloride in 79.2% yield.

[References]

[1] Patent: EP1398310, 2004, A1. Location in patent: Page 17
[2] Patent: EP1398310, 2004, A1. Location in patent: Page 17
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