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Merck
CN

525022

4-氨基吲哚

97%

别名:

4-吲哚胺

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关于此项目

经验公式(希尔记法):
C8H8N2
化学文摘社编号:
分子量:
132.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
114919
Assay:
97%
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assay

97%

mp

106-109 °C (lit.)

SMILES string

Nc1cccc2[nH]ccc12

InChI

1S/C8H8N2/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,9H2

InChI key

LUNUNJFSHKSXGQ-UHFFFAOYSA-N

General description

4-Aminoindole is an indole derivative. Its cytokinin activity has been assessed by tobacco pith callus bioassay. 4-Aminoindole can be prepared by reacting 2,6-dinitrotoluene and N,N-dimethylformamide dimethylacetal in anhydrous DMF.

Application

4-Aminoindole may be used to synthesize:
  • macrolactam tumour promoter indolactam V
  • tricyclic structure of 2-substituted-pyrrolo[2,3-h]quinolin-4-one
  • 4-azidoindole
Reactant for preparation of:
  • Inhibitors of bacterial thymidylate synthase
  • Mimetics of non-alkaloid toxin lignan anticancer and antiviral agent Podophyllotoxin (PPT)
  • Inhibitors of Gli1-mediated transcription in the Hedgehog pathway
  • Protein kinase C θ (PKCθ) inhibitors
  • Indolic non-peptidic HIV protease inhibitors
  • Transient receptor potential cation channel subfamily V member 1 (TRPV1) antagonists
  • Cyclooxygenase-2 (COX-2) and lipoxygenase (LOX) inhibitors
  • 11β-hydroxysteroid dehydrogenase 1 (11β-HSD1) inhibitors
  • Short chain 4-substituted indoles as potent αvβ3 antagonist
  • Ligands of serotonin transporter and 5-HT1A receptors


pictograms

Exclamation mark

signalword

Warning

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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