所有图片(1)
别名:
1-(tert-Butoxycarbonyl)indole, 1-Indolecarboxylic acid tert-butyl ester, N-tert-Butoxycarbonylindole, N-Butyloxycarbonylindole
经验公式（希尔记法）:
C13H15NO2
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检测方案
97%
折射率
n20/D 1.543 (lit.)
bp
201 °C (lit.)
密度
1.07 g/mL at 25 °C (lit.)
SMILES字符串
CC(C)(C)OC(=O)n1ccc2ccccc12
InChI
1S/C13H15NO2/c1-13(2,3)16-12(15)14-9-8-10-6-4-5-7-11(10)14/h4-9H,1-3H3
InChI key
OWPIFQXNMLDXKW-UHFFFAOYSA-N
应用
Reactant for preparation of:
- Potent plant-growth inhibitors
- Cannabinoid CB2 receptor ligands
- Analogues of isomeridianin G and evaluation as GSK-3β inhibitors
- Inhibitor of the Yersinia pestis salicylate adenylation domain YbtE
- Cholecystokinin-2 receptor antagonists
- Antileishmanial agents
- Reactant for:
- Palladium-catalyzed Suzuki-Miyaura cross coupling reactions
- Friedel-Crafts alkylation reactions
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
Solid-Phase Dendrimer Chemistry
Aldrichimica Acta, 34(3) (3001)
Eva Schendera et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(1), 269-274 (2019-09-26)
A metal-free, photoinduced aerobic tandem amine dehydrogenation/Povarov cyclization/aromatization reaction between N-aryl glycine esters and indoles leads to tetracyclic 11H-indolo[3,2-c]quinolines under mild conditions and with high yields. The reaction can be performed by using molecular iodine along with visible light, or
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