ChemicalBook--->CAS DataBase List--->89381-13-5

89381-13-5

89381-13-5 Structure

89381-13-5 Structure
IdentificationMore
[Name]

2-AMINO CYCLOPENTANOL
[CAS]

89381-13-5
[Synonyms]

2-AMINO CYCLOPENTANOL
Cyclopentanol,2-amino-(6CI,7CI,9CI)
trans-2-Amino-cyclopentanol
[Molecular Formula]

C5H11NO
[MDL Number]

MFCD00100903
[Molecular Weight]

101.15
[MOL File]

89381-13-5.mol
Chemical PropertiesBack Directory
[Boiling point ]

114-115℃ (13 Torr)
[density ]

1.0617 g/cm3(Temp: 15 °C)
[refractive index ]

1.4965 (589.3 nm 15℃)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

14.93±0.40(Predicted)
[Appearance]

Colorless to light yellow Liquid
[CAS DataBase Reference]

89381-13-5(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

2-Aminocyclopentanol can be used as a pharmaceutical synthesis intermediate. It can be prepared from cyclopentane oxide as a reaction raw material. It can be used to prepare 5-methyl-2-(pyridin-2-ylamino)-8H-pyrido[2,3-d]pyrimidin-7-one compounds. It can also be used to prepare drugs for treating diseases related to cyclin-dependent kinase signaling pathways.
Safety DataBack Directory
[Symbol(GHS) ]


GHS05,GHS07,GHS09
[Signal word ]

Danger
[Hazard statements ]

H302-H314-H410
[Precautionary statements ]

P264-P270-P301+P312-P280-P330-P501-P303+P361+P353-P304+P340-P310-P305+P351+P338-P273-P391
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[RIDADR ]

UN3082
[HazardClass ]

9
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO CYCLOPENTANOL(89381-13-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

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

672310-36-0

Cyclopentanol,2-amino-,(1S,2S)-(9CI)

930-45-0

General procedure for the synthesis of (1S,2S)-2-aminocyclopentanol from the compound (CAS:672310-36-0): 0.900 g (3.82 mmol) of (S,S)-2-benzyloxycarbonylaminocyclopentanol and 0.36 g of 5% palladium-carbon catalyst were added to the reaction system in a 50 mL autoclave. Under nitrogen protection, 4.5 mL of degassed methanol was added to the reaction system. The reaction mixture was stirred at 50 °C for 3 hours under hydrogen pressure of 2 MPa. Upon completion of the reaction, the palladium-carbon catalyst was removed by diatomaceous earth filtration, and the filtrate was concentrated by rotary evaporator to give 0.59 g of crude product. The product was determined to have an enantiomeric excess (ee) percentage of more than 99%. The 1H-NMR (200 MHz, CDCl3) data of the product were as follows: δ 1.2-1.3 (m, 1H), 1.5 (m, 1H), 1.6-1.7 (m, 2H), 1.9-2.0 (m, 2H), 2.3-2.5 (br, 3H), 3.0 (m, 1H), 3.7 (m, 1H).

[References]

[1] Patent: EP1398310, 2004, A1. Location in patent: Page 16-17
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