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1H-Indol-1-amine

Base Information
  • Chemical Name:1H-Indol-1-amine
  • CAS No.:53406-38-5
  • Molecular Formula:C8H8N2
  • Molecular Weight:132.165
  • Hs Code.:2933998090
  • Mol file:53406-38-5.mol
1H-Indol-1-amine

Synonyms:1-Aminoindole;

Suppliers and Price of 1H-Indol-1-amine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1-Aminoindole
  • 100mg
  • $ 75.00
  • SynQuest Laboratories
  • 1H-Indol-1-amine 95%
  • 5 g
  • $ 808.00
  • SynQuest Laboratories
  • 1H-Indol-1-amine 95%
  • 1 g
  • $ 272.00
  • Matrix Scientific
  • 1-Aminoindole 95+%
  • 25g
  • $ 885.00
  • Matrix Scientific
  • 1-Aminoindole 95+%
  • 1g
  • $ 160.00
  • Matrix Scientific
  • 1-Aminoindole 95+%
  • 5g
  • $ 480.00
  • Crysdot
  • 1-Aminoindole 95+%
  • 10g
  • $ 335.00
  • Chemcia Scientific
  • Indol-1-ylamine 97%
  • 5 G
  • $ 395.00
  • Apolloscientific
  • 1H-Indol-1-amine 95%
  • 5g
  • $ 505.00
  • Apolloscientific
  • 1H-Indol-1-amine 95%
  • 1g
  • $ 170.00
Total 50 raw suppliers
Chemical Property of 1H-Indol-1-amine
Chemical Property:
  • Vapor Pressure:0.00146mmHg at 25°C 
  • Melting Point:40 °C 
  • Refractive Index:1.638 
  • Boiling Point:296.208 °C at 760 mmHg 
  • PKA:7.05±0.70(Predicted) 
  • Flash Point:132.942 °C 
  • PSA:30.95000 
  • Density:1.183 g/cm3 
  • LogP:1.93630 
  • Storage Temp.:2-8°C(protect from light) 
Purity/Quality:

98% *data from raw suppliers

1-Aminoindole *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1H-Indol-1-amine

There total 8 articles about 1H-Indol-1-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

Guidance literature:
Guidance literature:
indole; hydroxylamine-O-sulfonic acid; With potassium tert-butylate; In 1-methyl-pyrrolidin-2-one; at 10 - 30 ℃; for 3.125h; Inert atmosphere; Large scale reaction;
Large scale reaction;
DOI:10.1021/op100330h
Guidance literature:
indole; With potassium tert-butylate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
With chloroamine; tert-butyl methyl ether; In N,N-dimethyl-formamide; at 20 ℃; for 0.25h;
DOI:10.1021/jo035587p
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