(1S,2S)-trans-N-Boc-2-aminocyclopentanol

(1S,2S)-trans-N-Boc-2-aminocyclopentanol Basic information
Product Name:(1S,2S)-trans-N-Boc-2-aminocyclopentanol
Synonyms:(1S,2S)-trans-N-Boc-2-aminocyclopentanol;tert-butyl (1S,2S)-2-hydroxycyclopentylcarbamate;((1S,2S)-2-Hydroxycyclopentyl)carbamic acid tert-butyl ester;tert-Butyl N-((2S,1S)-2-hydroxycyclopentyl)carbamate;(1S,2S)-trans-N-Boc-2-aminocyclopentanol 99%;(1S,2S)-2-(Boc-amino)cyclopentanol;Carbamic acid,N-[(1S,2S)-2-hydroxycyclopentyl]-, 1,1-dimethylethyl ester;tert-butyl (1S,2S)-2-hydroxycyclopentyl
CAS:145106-43-0
MF:C10H19NO3
MW:201.26
EINECS:
Product Categories:apis;Amino Alcohols;Chiral Building Blocks;Organic Building Blocks
Mol File:145106-43-0.mol
(1S,2S)-trans-N-Boc-2-aminocyclopentanol Structure
(1S,2S)-trans-N-Boc-2-aminocyclopentanol Chemical Properties
Melting point 87.0℃
Boiling point 320.8±31.0 °C(Predicted)
density 1.08±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. Sealed in dry,Room Temperature
pka12.09±0.40(Predicted)
BRN 5810036
Safety Information
Hazard Codes Xn,N
Risk Statements 22-50
Safety Statements 61
RIDADR UN 3077 9/PG 3
WGK Germany 3
MSDS Information
(1S,2S)-trans-N-Boc-2-aminocyclopentanol Usage And Synthesis
UsesReactant for:
  • Asymmetric synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors via stereoselective thioesterification, thioetherification, hydrolysis, heterocyclization and amination
(1S,2S)-trans-N-Boc-2-aminocyclopentanol Preparation Products And Raw materials
Raw materials(1S,2S)-trans-2-Aminocyclopentanol hydrochloride-->Di-tert-butyl dicarbonate

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