527246
N-(叔丁氧基羰基)-4-溴苯胺
97%
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关于此项目
线性分子式:
BrC6H4NHCO2C(CH3)3
化学文摘社编号:
分子量:
272.14
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
97%
mp
103-106 °C (lit.)
官能团
amine
bromo
SMILES字符串
CC(C)(C)OC(=O)Nc1ccc(Br)cc1
InChI
1S/C11H14BrNO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
InChI key
VLGPDTPSKUUHKR-UHFFFAOYSA-N
一般描述
N-(tert-Butoxycarbonyl)-4-bromoaniline is an N-(tert-butyloxycarbonyl) [N-BOC] protected 4-bromo aniline. Due to the presence of BOC protection, it serves as an ideal substrate for Suzuki coupling reactions. It affords biaryls via reaction with pyridine or 3-benzaldehyde boronic acids.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Coutts IGC, et al.
Tetrahedron Letters, 38, 5563-5563 (1997)
M Lamothe et al.
Journal of medicinal chemistry, 40(22), 3542-3550 (1997-11-14)
The synthesis and binding affinity at cloned h5-HT1D, h5-HT1D, and h5-HT1A receptors of 3-[3-(N,N-dimethylamino)propyl]-4-hydroxy- N-[4-(pyridin-4-yl)phenyl]benzamide (2, GR-55562) and four O-methylated analogs are described. The functional activity of these compounds was determined at the h5-HT1B receptor using a [35S]GTP gamma S
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