557749
N-Boc-5-溴吲哚
97%
别名:
5-溴吲哚-1-羧酸叔丁酯
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关于此项目
经验公式（希尔记法）:
C13H14BrNO2
化学文摘社编号:
分子量:
296.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
Quality Segment
assay
97%
form
solid
mp
56-57 °C (lit.)
functional group
bromo
SMILES string
CC(C)(C)OC(=O)n1ccc2cc(Br)ccc12
InChI
1S/C13H14BrNO2/c1-13(2,3)17-12(16)15-7-6-9-8-10(14)4-5-11(9)15/h4-8H,1-3H3
InChI key
PBWDRTGTQIXVBR-UHFFFAOYSA-N
General description
N-Boc-5-bromoindole can undergo Sonogashira coupling reaction with N,N-diisopropylprop-2-ynylamine to afford the corresponding propargylic diisopropylamine. N-Boc-5-bromoindole is formed as an intermediate during the synthesis of 2-(5-substituted-1H-indol-3-yl)-N-hydroxyacetamide derivatives.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Sylvain Petit et al.
ChemMedChem, 4(2), 261-275 (2008-12-05)
The lead compound 5-bromoindolyl-3-acetohydroxamic acid (10) was recently identified as a potent inhibitor of bacterial peptide deformylases (PDFs). The synthesis and associated activities of new variants were investigated at position 5 to optimize the fit at the S1' subsite and
Hiroyuki Nakamura et al.
The Journal of organic chemistry, 70(6), 2357-2360 (2005-03-12)
[reaction: see text] Propargylic diisopropylamines containing heterocycles, which were prepared readily from heterocyclic bromides and propargyldiisopropylamine by the Sonogashira coupling reaction, underwent the allene transformation reaction in the presence of Pd(2)(dba)(3).CHCl(3) catalyst (2.5 mol %) and 1,2-bis[bis(pentafluorophenyl)phosphino]ethane (10 mol %)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 557749-25G-A | 04061832242460 |
| 557749-5G-A | 04061832242477 |