145106-43-0

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145106-43-0 Structure

Identification	Back Directory
[Name] (1S,2S)-trans-N-Boc-2-aminocyclopentanol
[CAS] 145106-43-0
[Synonyms] (1S,2S)-2-(Boc-amino)cyclopentanol tert-butyl (1S,2S)-2-hydroxycyclopentyl (1S,2S)-trans-N-Boc-2-aminocyclopentanol (1S,2S)-trans-N-Boc-2-aminocyclopentanol 99% tert-butyl (1S,2S)-2-hydroxycyclopentylcarbamate ert-butylN-[(1S,2S)-2-hydroxycyclopentyl]carbamate (1S,2S)-trans-N-Boc-2-aminocyclopentanol USP/EP/BP tert-Butyl N-((2S,1S)-2-hydroxycyclopentyl)carbamate ((1S,2S)-2-Hydroxycyclopentyl)carbamic acid tert-butyl ester Carbamic acid,N-[(1S,2S)-2-hydroxycyclopentyl]-, 1,1-dimethylethyl ester
[Molecular Formula] C10H19NO3
[MDL Number] MFCD11656038
[MOL File] 145106-43-0.mol
[Molecular Weight] 201.26

Safety Data	Back Directory
[Symbol(GHS) ] GHS07,GHS09
[Signal word ] Warning
[Hazard statements ] H302-H400
[Precautionary statements ] P273-P301+P312+P330
[Hazard Codes ] Xn,N
[Risk Statements ] 22-50
[Safety Statements ] 61
[RIDADR ] UN 3077 9/PG 3
[WGK Germany ] 3

Hazard Information	Back Directory
[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

Spectrum Detail	Back Directory
[Spectrum Detail] (1S,2S)-trans-N-Boc-2-aminocyclopentanol(145106-43-0)¹HNMR

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