(1S,2S)-TRANS-N-BOC-2-AMINOCYCLOPENTANOL ,145106-43-0 _ChemCD

(1S,2S)-TRANS-N-BOC-2-AMINOCYCLOPENTANOL

basic_info
Product_Name：	(1S,2S)-TRANS-N-BOC-2-AMINOCYCLOPENTANOL
CAS：	145106-43-0
EnglishSynonyms：	TERT-BUTYL (1S,2S)-2-HYDROXYCYCLOPENTYLCARBAMATE ; TERT-BUTYL N-[(1S,2S)-2-HYDROXYCYCLOPENTYL]CARBAMATE ; 1-N-BOC-(1S,2S)-1-AMINOCYCLOPENTAN-2-OL ; TERT-BUTYL N-((2S,1S)-2-HYDROXYCYCLOPENTYL)CARBAMATE ; (1S,2S)-TRANS-N-BOC-2-AMINOCYCLOPENTANOL ; (S,S)-(-)-2-N-BOC-AMINOCYCLOPENTANOL ; ((1S,2S)-2-HYDROXYCYCLOPENTYL)CARBAMIC ACID TERT-BUTYL ESTER
pro_mdlNumber：	MFCD11656038
pro_acceptors：	4
pro_donors：	2
pro_smile：	CC(C)(C)OC(=O)N[C@H]1CCC[C@@H]1O
InChi：	InChI=1S/C10H19NO3/c1-10(2,3)14-9(13)11-7-5-4-6-8(7)12/h7-8,12H,4-6H2,1-3H3,(H,11,13)/t7-,8-/m0/s1
InChiKey：	InChIKey=CGZQRJSADXRRKN-YUMQZZPRSA-N
property
Comments：	APPLICATION: REACTANT FOR: ASYMMETRIC SYNTHESIS OF CONSTRAINED (-)-S-ADENOSYL-L-HOMOCYSTEINE (SAH) ANALOGS AS DNA METHYLTRANSFERASE INHIBITORS VIA STEREOSELECTIVE THIOESTERIFICATION, THIOETHERIFICATION, HYDROLYSIS, HETEROCYCLIZATION AND AMINATION ASSAY METHOD: GC RIDADR: UN 3077 9/PG 3 STORAGE TEMPERATURE: 2-8 DEG C WGK: 3
Information：	OPTICAL PURITY: ENANTIOMERIC RATIO: =>95:5%
secure_info
secure_symbol：	GHS07 GHS09
secure_signal_word：	Warning
secure_risk_stmt：	H302-H400
secure_cautionary_stmt：	P273
secure_damage_code：	Xn,N
secure_risk_disclosure_stmt：	R:22-50
secure_security_stmt：	S:61
secure_wgk_germany：	3

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