57210
吲哚-3-甲醛
purum, ≥98.0% (T)
别名:
β-吲哚甲醛, 3-吲哚甲醛, 3-甲酰基吲哚, NSC 10118, 吲哚-3-甲醛
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关于此项目
经验公式（希尔记法）:
C9H7NO
化学文摘社编号:
分子量:
145.16
EC Number:
207-665-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
114117
MDL number:
InChI key
OLNJUISKUQQNIM-UHFFFAOYSA-N
InChI
1S/C9H7NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-6,10H
SMILES string
O=Cc1c[nH]c2ccccc12
grade
purum
assay
≥98.0% (T)
Application
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
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
S Muthu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 299-309 (2013-02-19)
Indole-3-Aldehyde is a new organic non-linear material having good second harmonic generation. The optimized molecular geometry, harmonic vibrational frequencies, infrared intensities of Indole-3-Aldehyde (I3A, C9H7NO) in the ground state were carried out by using density functional theory (B3LYP) method with
Deepa Sinha et al.
European journal of medicinal chemistry, 43(1), 160-165 (2007-05-29)
Eight novel heterocyclic Schiff bases derived from the condensation reactions of indole 3-carboxaldehyde with different l-amino acids (histidine, glutamic acid, aspartic acid, leucine, valine) as well as with some aminophenols, have been synthesized and characterized by various spectroscopic methods (IR
J S Biradar et al.
European journal of medicinal chemistry, 46(12), 6112-6118 (2011-10-22)
A rapid, efficient and environmental benign methodology for the preparation of 2,5-disubstituted indole analogues is developed. 2,5-Disubstituted indole-3-carboxaldehydes (1a-c) undergo Knoevenagel condensation with barbiturates (2 &4), thiazolidine-2,4-dione (6) and 3-methyl-1H-pyrazol-5(4H)-one (8) in solvent-free, NH(4)OAc catalyzed, microwave assisted reaction. Structures of
Gokce Gurkok et al.
Chemotherapy, 55(1), 15-19 (2008-11-01)
Indoles and hydrazone-type compounds constitute an important class of compounds for new drug development in order to discover an effective compound against multi-drug-resistant microbial infections. A series of indole-3-aldehyde and 5-bromoindole-3-aldehyde hydrazide and hydrazones was evaluated for their in vitro
Kakul Husain et al.
European journal of medicinal chemistry, 42(10), 1300-1308 (2007-04-20)
In continuation of our research on thiosemicarbazones and their metal complexes as antiamoebic agents, a new series of indole-3-carboxaldehyde thiosemicarbazones (TSC) 1-7 were prepared by condensing indole-3-carboxaldehyde with cycloalkylaminothiocarbonyl hydrazines. Their palladium(II) complexes of the [Pd(TSC)Cl2] type, were synthesized upon
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