Basic information Uses Safety Supplier Related

2-AMINO CYCLOPENTANOL

Basic information Uses Safety Supplier Related

2-AMINO CYCLOPENTANOL Basic information

Product Name:
2-AMINO CYCLOPENTANOL
Synonyms:
  • 2-AMINO CYCLOPENTANOL
  • Cyclopentanol,2-amino-(6CI,7CI,9CI)
  • Cyclopentanol, 2-aMino-
  • 2-AMinocyclopentanol, 95+%
  • trans-2-Amino-cyclopentanol
  • 1-AMino-2-hydroxycyclopentane
  • 2-HydroxycyclopentylaMine
  • 2-aminocyclopentan-1-ol
CAS:
89381-13-5
MF:
C5H11NO
MW:
101.15
Product Categories:
  • pharmacetical
  • VARIOUSAMINE
Mol File:
89381-13-5.mol
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2-AMINO CYCLOPENTANOL Chemical Properties

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)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
RIDADR 
UN3082
HazardClass 
9
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2-AMINO CYCLOPENTANOL Usage And Synthesis

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.

Synthesis

672310-36-0

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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