2-Amino cyclopentanol

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2-Amino cyclopentanol manufacturers

  • 2-AMINO CYCLOPENTANOL
  • 2-AMINO CYCLOPENTANOL pictures
  • $2.00
  • 2020-01-08
  • CAS:89381-13-5
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 100g , 1kg, 5kg , 50kg
2-Amino cyclopentanol Basic information
Uses
Product Name:2-Amino cyclopentanol
Synonyms: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;2-AminocycL
CAS:89381-13-5
MF:C5H11NO
MW:101.15
EINECS:
Product Categories:VARIOUSAMINE;pharmacetical
Mol File:89381-13-5.mol
2-Amino cyclopentanol Structure
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
pka14.93±0.40(Predicted)
AppearanceColorless to light yellow Liquid
CAS DataBase Reference89381-13-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
RIDADR UN3082
HazardClass 9
MSDS Information
2-Amino cyclopentanol Usage And Synthesis
Uses2-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
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
2-Amino cyclopentanol Preparation Products And Raw materials
Raw materialsCarbamic acid, N-[(1R,2R)-2-hydroxycyclopentyl]-, phenylmethyl ester-->Methanol-->Hydrogen
Tag:2-Amino cyclopentanol(89381-13-5) Related Product Information
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