4-Hydroxy-N,N-diisopropyltryptamine

Base Information

• Chemical Name: 4-Hydroxy-N,N-diisopropyltryptamine
• CAS No.: 132328-45-1
• Molecular Formula: C16H24N2O
• Molecular Weight: 260.379
• Hs Code.: 2933990090
• Mol file: 132328-45-1.mol

Synonyms:N,N-Diisopropyl-4-hydroxytryptamine;

Chemical Property of 4-Hydroxy-N,N-diisopropyltryptamine

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.593
• Boiling Point: 424.911 °C at 760 mmHg
• PKA: 9.83±0.40(Predicted)
• Flash Point: 210.779 °C
• PSA: 39.26000
• Density: 1.084 g/cm³
• LogP: 3.53480

Purity/Quality:

99% min ^*data from raw suppliers

4-HYDROXY-N,N-DIISOPROPYLTRYPTAMINE 98.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 4-Hydroxy-N,N-diisopropyltryptamine

There total 4 articles about 4-Hydroxy-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:

Reference yield: 52.0%

1-((p-methoxyphenyl)amino)-2-(((p-methoxyphenyl)imino)methyl)acenaphthylene hydrochloride (132297-88-2) → 10-methoxyacenaphtho<1,2-b>quinoline (132297-89-3)

Guidance literature:

at 225 - 230 ℃;

DOI:10.1021/jo00006a063

Reference yield:

2-chloroacenaphthylene-1-carbaldehyde (13152-84-6) → 10-methoxyacenaphtho<1,2-b>quinoline (132297-89-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 97 percent / 2 N HCl / ethanol / 3 h / Ambient temperature

2: 52 percent / 225 - 230 °C

With hydrogenchloride; In ethanol;

DOI:10.1021/jo00006a063

Reference yield:

4-methoxy-aniline (104-94-9) → 10-methoxyacenaphtho<1,2-b>quinoline (132297-89-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 97 percent / 2 N HCl / ethanol / 3 h / Ambient temperature

2: 52 percent / 225 - 230 °C

With hydrogenchloride; In ethanol;

DOI:10.1021/jo00006a063

upstream raw materials:

1-((p-methoxyphenyl)amino)-2-(((p-methoxyphenyl)imino)methyl)acenaphthylene hydrochloride

2-chloroacenaphthylene-1-carbaldehyde

4-methoxy-aniline

Refernces

• 1、 Repke,Ferguson,Bates. "Psilocin analogs. I. Synthesis of 3 [2 dialkylamino)ethyl] and 3 [2 (Cycloalkylamino)ethyl] indol 4 ols". . p. 71 - 74. Retrieved 2007/10/04.