(2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANE

CAS No.
286019-82-7 ;98737-29-2
CCD No.
CCD00305602
Formula
C15 H21 N O3
MolWeight
263.335

Basic Information

Product Name: (2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANE
CAS: 286019-82-7 ;98737-29-2
English Synonyms: CARBAMIC ACID, [(1S)-1-(2S)-OXIRANYL-2-PHENYLETHYL]-, 1,1-DIMETHYLETHYL ESTER ; [(1S)-1-((2S)-OXIRANYL)-2-PHENYLETHYL]CARBAMIC ACID TERT-BUTYL ESTER ; (2S,3S)-3-(N-BOC-AMINO)-1-OXIRANE-4-PHENYLBUTANE ; [1(S)-BENZYL-2(S),3-EPOXYPROPYL]-CARBAMIC ACID TERT-BUTYL ESTER ; N-[(1S)-1-[(2S)-2-OXIRANYL]-2-PHENYLETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER ; TERT-BUTYL [S-(R*,R*)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; (2S,3S)-1,2-EPOXY-3-(TERT-BUTOXYCARBONYLAMINO)-4-PHENYLBUTANE ; (2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANE ; TERT-BUTYL [(S)-1-((S)-2-OXIRANYL)-2-PHENYLETHYL]CARBAMATE ; (2S, 3S)-(-)-3-TERT-BUTOXYCARBONYLAMINO-1, 2-EPOXY-4-PHENYLBUTANE ; (2S,3S)-3-(BOC-AMINO)-1,2-EPOXY-4-PHENYLBUTANE ; (1S,2S)-(1-OXIRANYL-2-PHENYL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER ; 2S,3S-1,2-EPOXY-3-(T-BUTOXYCARBONYLAMINO)-4-PHENYLBUTANE ; (2S,3S)-(-)-3-(T-BOC-AMINO)-1,2-EPOXY-4-PHENYLBUTANE ; 3S-(T-BOC)AMINO-1,2-(S)-EPOXY-4-PHENYLBUTANE ; (2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANETERT-BUTYL ; TERT-BUTYL N-[(1S)-1-[(2S)-OXIRAN-2-YL]-2-PHENYLETHYL]CARBAMATE ; T-BUTYL [S-(R*,R*)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; (2S,3S)-N-BOC-3-AMINO-1,2-EPOXY-4-PHENYLBUTANE ; (2S,3S)-N-T-BOC-3-AMINO-1,2-EPOXY-4-PHENYLBUTANE ; TERT-BUTYL ((S)-(R,R))-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; TERT-BUTYL [(S)-1-[(S)-OXIRAN-2-YL]-2-PHENYLETHYL]CARBAMATE
MDL Number.: MFCD02258997
H bond acceptor: 4
H bond donor: 1
Smile: CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)[C@H]2CO2
InChi: InChI=1S/C15H21NO3/c1-15(2,3)19-14(17)16-12(13-10-18-13)9-11-7-5-4-6-8-11/h4-8,12-13H,9-10H2,1-3H3,(H,16,17)/t12-,13+/m0/s1
InChiKey: InChIKey=NVPOUMXZERMIJK-QWHCGFSZSA-N

Property

Melting Point: 125-127 DEG C(LIT)
Comments: APPLICATION: BUILDING BLOCK EMPLOYED IN THE SYNTHESIS OF HIV-1 PROTEASE INHIBITORS
APPLICATION: EMPLOYED IN SYNTHESIZING (HYDROXYETHYL)UREA PEPTIDOMIMETRICS AND ARYLSULFONAMIDES POSSESSING ANTI-HIV ACTIVITY
OPTICAL ACTIVITY: [ALPHA]23/D -7 DEG, C = 0.6 IN METHANOL
UNSPSC: 12352100
WGK: 3

Safety information

Symbol: GHS09 GHS09
Signal word: Warning
Hazard statements: H410
Precautionary statements: P273-P501
hazard symbol: N
Risk Code: R:50/53
Safe Code: S:60-61
WGK Germany: 3

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