Boc-L-丙氨醛结构式
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常用名 | Boc-L-丙氨醛 | 英文名 | Boc-L-alaninal |
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CAS号 | 79069-50-4 | 分子量 | 173.210 | |
密度 | 1.0±0.1 g/cm3 | 沸点 | 248.5±23.0 °C at 760 mmHg | |
分子式 | C8H15NO3 | 熔点 | 89 °C | |
MSDS | 美版 | 闪点 | 104.1±22.6 °C |
中文名 | Boc-L-丙氨醛 |
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英文名 | tert-butyl N-[(2S)-1-oxopropan-2-yl]carbamate |
中文别名 | N-叔丁氧羰基-L-丙氨醛 |
英文别名 | 更多 |
密度 | 1.0±0.1 g/cm3 |
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沸点 | 248.5±23.0 °C at 760 mmHg |
熔点 | 89 °C |
分子式 | C8H15NO3 |
分子量 | 173.210 |
闪点 | 104.1±22.6 °C |
精确质量 | 173.105194 |
PSA | 55.40000 |
LogP | 1.23 |
外观性状 | Powder | White to yellow |
蒸汽压 | 0.0±0.5 mmHg at 25°C |
折射率 | 1.436 |
储存条件 | −20°C |
水溶解性 | 可溶于:甲醇 |
个人防护装备 | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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危害码 (欧洲) | Xi |
危险品运输编码 | NONH for all modes of transport |
WGK德国 | 3 |
Boc-L-丙氨醛上游产品 9 | |
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Boc-L-丙氨醛下游产品 8 | |
Synthesis of the C(26)-C(32) Oxazole Fragment of Calyculin C: A Test Case for Oxazole Syntheses.
J. Org. Chem. 63 , 92-98, (1998) The synthesis of the C(26)-C(32) oxazole fragment 4 and its C(32) epimer 20 of serine/threonine protein phosphatase PP1 and PP2A inhibitor calyculin C is presented. The syn methyl arrangement in 4 was... |
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Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal.
Org. Lett. 7 , 1593-1596, (2005) [reaction: see text] Additions of chiral allenylzinc and indium reagents to N-Boc alaninal were examined as a possible route to a C20-C26 segment of superstolide A. Allenylzinc reagents, prepared in s... |
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Practical syntheses of a CXCR3 antagonist.
J. Org. Chem. 76 , 1767-1774, (2011) Two new, reliable syntheses of a pyrido[2,3-d]-pyrimidine inhibitor of the CXCR3 receptor are described. A nine-step synthesis of the CXCR3 inhibitor (1) from 2-aminonicotinic acid was demonstrated on... |
tert-Butyl [(2S)-1-oxopropan-2-yl]carbamate |
Boc-L-alanine aldehyde |
(S)-tert-Butyl (1-oxopropan-2-yl)carbamate |
Carbamic acid, N-[(1S)-1-methyl-2-oxoethyl]-, 1,1-dimethylethyl ester |
Boc-alaninal |
Boc-Ala-Aldehyde |
2-Methyl-2-propanyl (1-oxo-2-propanyl)carbamate |
N-T-BOC-L-ALANINAL |
2-Methyl-2-propanyl [(2S)-1-oxo-2-propanyl]carbamate |
N-Boc-L-alaninal |
Boc-L-alaninal |
boc-L-alanine |
Carbamic acid, N-(1-methyl-2-oxoethyl)-, 1,1-dimethylethyl ester |
Boc-Ala-H |