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Merck
CN

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:
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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

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历史批次信息供参考:

分析证书(COA)

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Tian-Lin Yang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 67(2), 568-571 (2006-09-22)
A new Schiff base ligand with tripodal structure, N,N',N''-tri-(3-indolemethanal)-triaminotriethylamine (L), and its complex with terbium was synthesized. The complex was characterized by element analysis, IR spectra, mass spectra, thermal analysis and molar conductivity. The terbium ion was found to coordinate
Kakul Husain et al.
European journal of medicinal chemistry, 43(9), 2016-2028 (2008-01-29)
Reaction of 3-indole carboxaldehyde with aminothiocarbonyl hydrazines resulted in the formation of 3-indole carboxaldehyde thiosemicarbazones (TSCs) 1-13. The synthesized thiosemicarbazones were used as ligands in the formation of [Pd(TSC)Cl2] complexes with palladium(II) metal ion precursor, [Pd(DMSO)2Cl2]. The chemical structures of
Tudor Rosu et al.
European journal of medicinal chemistry, 53, 380-389 (2012-04-21)
Six new Cu(II), Ni(II), and VO(II) complexes (1-6) with Schiff base 1-phenyl-2,3-dimethyl-4-(1H-indole-3-carboxaldehyde)-3-pyrazolin-5-one (HL) were synthesized. The Schiff base was prepared through the condensation of 1-phenyl-2,3-dimethyl-4-amino-3-pyrazolin-5-one (antipyrine) with 1H-indole-3-carboxaldehyde. The new obtained compounds were characterized by (1)H NMR, (13)C NMR, UV-VIS
Anna M Vetrano et al.
The Journal of biological chemistry, 280(42), 35372-35381 (2005-08-05)
Catalase is a highly conserved heme-containing antioxidant enzyme known for its ability to degrade hydrogen peroxide into water and oxygen. In low concentrations of hydrogen peroxide, the enzyme also exhibits peroxidase activity. We report that mammalian catalase also possesses oxidase
Juan Nogales et al.
The Journal of biological chemistry, 280(42), 35382-35390 (2005-07-21)
In this work we have characterized the galA gene product from Pseudomonas putida KT2440, a ring-cleavage dioxygenase that acts specifically on gallate to produce 4-oxalomesaconate. The protein is a trimer composed by three identical subunits of 47.6 kDa (419 amino

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