Boc-L-丙氨醛

更新时间:2024-01-03 22:24:40

Boc-L-丙氨醛结构式
Boc-L-丙氨醛结构式
品牌特惠专场
常用名 Boc-L-丙氨醛 英文名 Boc-L-alaninal
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

 Boc-L-丙氨醛名称

中文名 Boc-L-丙氨醛
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

 Boc-L-丙氨醛物理化学性质

密度 1.0±0.1 g/cm3
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

 Boc-L-丙氨醛MSDS

 Boc-L-丙氨醛安全信息

个人防护装备 Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
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-丙氨醛合成线路

 Boc-L-丙氨醛文献3

更多文献
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...

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...

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...

 Boc-L-丙氨醛英文别名

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