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4-Acetoxy-N,N-diisopropyltryptamine

Base Information
  • Chemical Name:4-Acetoxy-N,N-diisopropyltryptamine
  • CAS No.:936015-60-0
  • Molecular Formula:C18H26N2O2
  • Molecular Weight:302.417
  • Hs Code.:2933990090
  • Mol file:936015-60-0.mol
4-Acetoxy-N,N-diisopropyltryptamine

Synonyms:[3-[2-[Di(propan-2-yl)amino]ethyl]-1H-indol-4-yl] acetate;4-Acetoxy-N,N-diisopropyltryptamine;

Suppliers and Price of 4-Acetoxy-N,N-diisopropyltryptamine
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
  • American Custom Chemicals Corporation
  • 4-ACETOXY-N,N-DIISOPROPYLTRYPTAMINE 95.00%
  • 5MG
  • $ 499.54
Total 58 raw suppliers
Chemical Property of 4-Acetoxy-N,N-diisopropyltryptamine
Chemical Property:
  • Appearance/Colour:slightly off-white powder 
  • Vapor Pressure:4.88E-08mmHg at 25°C 
  • Refractive Index:1.563 
  • Boiling Point:442.789 °C at 760 mmHg 
  • PKA:16.61±0.30(Predicted) 
  • Flash Point:221.591 °C 
  • PSA:45.33000 
  • Density:1.082 g/cm3 
  • LogP:3.75450 
Purity/Quality:

99% *data from raw suppliers

4-ACETOXY-N,N-DIISOPROPYLTRYPTAMINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-Acetoxy-N,N-diisopropyltryptamine

There total 1 articles about 4-Acetoxy-N,N-diisopropyltryptamine 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:
Guidance literature:
acetic acid 1H-indol-4-yl ester; With oxalyl dichloride; In tert-butyl methyl ether;
With lithium aluminium tetrahydride; In tetrahydrofuran;
upstream raw materials:

acetic acid 1H-indol-4-yl ester

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