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| (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 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 | pka | 12.09±0.40(Predicted) | BRN | 5810036 |
Hazard Codes | Xn,N | Risk Statements | 22-50 | Safety Statements | 61 | RIDADR | UN 3077 9/PG 3 | WGK Germany | 3 |
| (1S,2S)-trans-N-Boc-2-aminocyclopentanol Usage And Synthesis |
Uses | Reactant for:
- Asymmetric synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors via stereoselective thioesterification, thioetherification, hydrolysis, heterocyclization and amination
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| (1S,2S)-trans-N-Boc-2-aminocyclopentanol Preparation Products And Raw materials |
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