2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol

Base Information

• Chemical Name: 2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol
• CAS No.: 19298-14-7
• Molecular Formula: C8H12N2O
• Molecular Weight: 152.196
• Hs Code.: 2922199090
• DSSTox Substance ID: DTXSID90698233
• Mol file: 19298-14-7.mol

Synonyms:DTXSID90698233;2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol

Chemical Property of 2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol

Chemical Property:

• Boiling Point: 360.771 °C at 760 mmHg
• Flash Point: 171.988 °C
• PSA: 72.27000
• Density: 1.216 g/cm³
• LogP: 0.92020
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 154.110613074
• Heavy Atom Count: 11
• Complexity: 189

Purity/Quality:

99% ^*data from raw suppliers

2-[(4-Aminophenyl)amino]ethan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(C(C=C1)(CCO)N)N

Technology Process of 2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol

There total 6 articles about 2-(1,6-Diaminocyclohexa-2,4-dien-1-yl)ethan-1-ol 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: 97.0%

N-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)phenylene-1,4-diamine (890051-96-4) → 4-di[(2-hydroxyethyl)amino]-aniline (19298-14-7)

Guidance literature:

With hydrogen; palladium 10% on activated carbon; In ethanol; at 20 ℃; under 760.051 Torr; Inert atmosphere;

Reference yield: 70.0%

[1,3]-dioxolan-2-one (96-49-1) + 1,4-phenylenediamine (106-50-3) → N,N'-bis-(2'-hydroxyethyl)-p-phenylenediamine + 4-di[(2-hydroxyethyl)amino]-aniline (19298-14-7)

Guidance literature:

With Na-Y zeolite; In Triethylene glycol dimethyl ether; for 2h; Heating;

DOI:10.1055/s-2006-939697

Reference yield:

N-(2-hydroxyethyl)-4-nitroaniline (1965-54-4) → 4-di[(2-hydroxyethyl)amino]-aniline (19298-14-7)

Guidance literature:

With hydrogenchloride; tin;

DOI:10.1021/ja01875a002

upstream raw materials:

N-(2-hydroxyethyl)-4-nitroaniline

[1,3]-dioxolan-2-one

1,4-phenylenediamine

ethanolamine

Downstream raw materials:

5-chloro-N-(2-{4-[(2-hydroxyethyl)amino]phenyl}-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl)thiophene-2-carboxamide

C₂₅H₂₄Cl₂N₄O₆S₂

2-{2-[1-(5-chlorothiophen-2-yl)-N-{4-[(5S)-5-{[(5-chlorothiophen-2-yl)formamido]methyl}-2-oxo-1,3-oxazolidin-3-yl]phenyl}formamido]ethoxy}acetic acid

2-(4-(4-(cyclopentylamino)-5-nitropyrimidin-2-ylamino)phenylamino)ethanol

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