Quality Level
assay
97%
form
solid
mp
193-198 °C (lit.)
functional group
aldehyde
SMILES string
O=Cc1c[nH]c2ccccc12
InChI
1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
InChI key
OLNJUISKUQQNIM-UHFFFAOYSA-N
General description
吲哚-3-甲醛可进行席夫碱缩合,从而形成多功能二氧化硅纳米载体和磁性纳米粒子。
Application
吲哚-3-甲醛可用于制备带有NR1R2基团的吲哚植物抗毒素环油菜素的类似物。它也被用作合成高阶吲哚的起始材料,包括异吲哚[2,1-a]吲哚、 aplysinopsins、 以及4-取代四氢苯并[cd]吲哚。
其是制备如下化合物所需的反应物:
- 镇痛剂
- 降糖药
- 色氨酸双加氧酶抑制剂吡啶基-乙烯基-吲哚(作为潜在的抗癌免疫调节剂)
- 抗菌和抗真菌剂
- 抗变形虫药和细胞毒性剂
- 登革病毒蛋白酶的抑制剂(在细胞培养中具有抗病毒活性)
- 姜黄素类似物(可能的抗增殖 & 抗炎剂)
- Bcl-2家族蛋白的抑制剂
- RNA聚合酶IIC末端结构域的抑制剂(作为抗肿瘤剂)
- TNF-α和IL-6的抑制剂(具有抗结核活性)
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Indian J. Chem. B, 33, 4-4 (1994)
Mariana Budovská et al.
Bioorganic & medicinal chemistry, 21(21), 6623-6633 (2013-09-10)
An effective synthesis of analogs of the indole phytoalexin cyclobrassinin with NR1R2 group instead of SCH3 was developed starting from indole-3-carboxaldehyde. The target compounds were prepared by spirocyclization of 1-Boc-thioureas with the formation of isolable spiroindoline intermediates, followed by the
Heterocycles, 38, 1479-1479 (1994)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 129445-5G | 04061838726230 |
| 129445-25G | 04061838726223 |