基本信息 |
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| 产品名称： | [(1S)-1-(2S)-环氧乙烷-2-苯基乙基]-氨基甲酸-(1,1-二甲基)乙酯 |
| CAS： | 98737-29-2 ;286019-82-7 |
| 中文同义词： | [(1S)-1-(2S)-环氧乙烷-2-苯基乙基]-氨基甲酸-(1,1-二甲基)乙酯 ; (2R,3S)-1,2-环氧-3-叔丁氧羰基氨基-4-苯基丁烷 ; (2S,3S)-1,2-环氧-3-(叔丁氧基羰基氨基)-4-苯丁烷 ; 3-菲羧酸,4b,5,6,7,8,8a,9,10-八氢-2-羟基-4b,8,8-三甲基-1-(1-甲基乙基)-,(4bS,8aS)- ; (2S,3S)-1,2-环氧-3-叔丁氧羰基氨基-4-苯基丁烷 |
| 英文同义词： | TERT-BUTYL [(S)-1-[(S)-OXIRAN-2-YL]-2-PHENYLETHYL]CARBAMATE ; CARBAMIC ACID, [(1S)-1-(2S)-OXIRANYL-2-PHENYLETHYL]-, 1,1-DIMETHYLETHYL ESTER ; (2S,3S)-3-(N-BOC-AMINO)-1-OXIRANE-4-PHENYLBUTANE ; (2S,3S)-N-T-BOC-3-AMINO-1,2-EPOXY-4-PHENYLBUTANE ; [(1S)-1-((2S)-OXIRANYL)-2-PHENYLETHYL]CARBAMIC ACID TERT-BUTYL ESTER ; TERT-BUTYL ((S)-(R,R))-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; 3S-(T-BOC)AMINO-1,2-(S)-EPOXY-4-PHENYLBUTANE ; TERT-BUTYL N-[(1S)-1-[(2S)-OXIRAN-2-YL]-2-PHENYLETHYL]CARBAMATE ; (2S, 3S)-(-)-3-TERT-BUTOXYCARBONYLAMINO-1, 2-EPOXY-4-PHENYLBUTANE ; (1S,2S)-(1-OXIRANYL-2-PHENYL-ETHYL)-CARBAMIC ACID TERT-BUTYL ESTER ; T-BUTYL [S-(R*,R*)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; N-[(1S)-1-[(2S)-2-OXIRANYL]-2-PHENYLETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER ; 2S,3S-1,2-EPOXY-3-(T-BUTOXYCARBONYLAMINO)-4-PHENYLBUTANE ; TERT-BUTYL [S-(R*,R*)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE ; [1(S)-BENZYL-2(S),3-EPOXYPROPYL]-CARBAMIC ACID TERT-BUTYL ESTER ; (2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANETERT-BUTYL ; (2S,3S)-3-(BOC-AMINO)-1,2-EPOXY-4-PHENYLBUTANE ; (2S,3S)-N-BOC-3-AMINO-1,2-EPOXY-4-PHENYLBUTANE ; (2S,3S)-1,2-EPOXY-3-(TERT-BUTOXYCARBONYLAMINO)-4-PHENYLBUTANE ; TERT-BUTYL [(S)-1-((S)-2-OXIRANYL)-2-PHENYLETHYL]CARBAMATE ; (2S,3S)-(-)-3-(T-BOC-AMINO)-1,2-EPOXY-4-PHENYLBUTANE ; (2S,3S)-1,2-EPOXY-3-(BOC-AMINO)-4-PHENYLBUTANE |
| MDL号： | MFCD02258997 |
| 氢键受体数量： | 4 |
| 氢键供体数量： | 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 |
性质 |
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| 熔点： | 125-127 DEG C(LIT) |
| 注解： | 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 |
安全信息 |
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| 符号： |
GHS09
|
| 信号词： | Warning |
| 危险声明： | H410 |
| 警示性声明： | P273-P501 |
| 危害码： | N |
| 风险声明： | R:50/53 |
| 安全声明： | S:60-61 |
| WGK德国： | 3 |
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