2,4,6-trimethoxyaniline Hydrochloride

Base Information

• Chemical Name: 2,4,6-trimethoxyaniline Hydrochloride
• CAS No.: 102438-99-3
• Molecular Formula: C9H13 N O3 . Cl H
• Molecular Weight: 219.668
• Hs Code.: 2922299090
• European Community (EC) Number: 823-173-1
• DSSTox Substance ID: DTXSID00377446
• Mol file: 102438-99-3.mol

Synonyms:2,4,6-trimethoxyaniline Hydrochloride;102438-99-3;2,4,6-trimethoxyaniline;hydrochloride;Benzenamine, 2,4,6-trimethoxy-, hydrochloride (1:1);2,4,6-TRIMETHOXYANILINEHYDROCHLORIDE;SCHEMBL5265528;DTXSID00377446;GRHAUEFIQOUKAY-UHFFFAOYSA-N;2,4,6-TRIMETHOXYANILINEHCL;MFCD00211326;AKOS005071449;SB79453;2,4,6 trimethoxy aniline mono HCl salt;2,4,6-Trimethoxyaniline (hydrochloride);8W-0406S;CS-0256305;FT-0680688;C14018;EN300-1717669;J-507080

Chemical Property of 2,4,6-trimethoxyaniline Hydrochloride

Chemical Property:

• Vapor Pressure: 0.000751mmHg at 25°C
• Melting Point: 220-225°
• Boiling Point: 306.9°Cat760mmHg
• Flash Point: 152.5°C
• PSA: 53.71000
• Density: 1.118g/cm³
• LogP: 2.67780
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 219.0662210
• Heavy Atom Count: 14
• Complexity: 140

Purity/Quality:

99%, ^*data from raw suppliers

2,4,6-Trimethoxyaniline hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC(=C(C(=C1)OC)N)OC.Cl

Technology Process of 2,4,6-trimethoxyaniline Hydrochloride

There total 2 articles about 2,4,6-trimethoxyaniline Hydrochloride 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: 98.0%

2,4,6-trimethoxyaniline (14227-17-9) → 2,4,6-trimethoxyaniline hydrochloride (102438-99-3)

Guidance literature:

With hydrogenchloride; In diethyl ether; dichloromethane; water; at 4 - 20 ℃; for 17h;

Reference yield:

2,4,6-trimethoxybenzamide (17483-54-4) → 2,4,6-trimethoxyaniline hydrochloride (102438-99-3)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; potassium permanganate; chlorine / water / 18 h / 0 - 20 °C

2: hydrogenchloride / diethyl ether; dichloromethane / 17 h / 0 - 20 °C

With hydrogenchloride; potassium permanganate; chlorine; In diethyl ether; dichloromethane; water;

DOI:10.1002/cmdc.201100318

Reference yield: 96.0%

2,4,6-trimethoxyaniline hydrochloride (102438-99-3) + 3-dodecyl-5-isoxazole acetic acid (159458-24-9) → 3-dodecyl-N-(2,4,6-trimethoxyphenyl)-5-isoxazole acetamide

Guidance literature:

3-dodecyl-5-isoxazole acetic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃; for 2h;

2,4,6-trimethoxyaniline hydrochloride; With triethylamine; In tetrahydrofuran; for 48h;

upstream raw materials:

2,4,6-trimethoxyaniline

2,4,6-trimethoxybenzamide

Downstream raw materials:

2,4,6-trimethoxyphenyl isocyanate

(Z)-N-(2,4,6-trimethoxyphenyl)-9-octadecenamide

2,2-Dimethyl-decanoic acid (2,4,6-trimethoxy-phenyl)-amide

2-Methyl-dodecanoic acid (2,4,6-trimethoxy-phenyl)-amide

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