4-(Aminomethyl)benzene-1,2-diol hydrochloride

Base Information

• Chemical Name: 4-(Aminomethyl)benzene-1,2-diol hydrochloride
• CAS No.: 1124-40-9
• Molecular Formula: C7H9NO2.ClH
• Molecular Weight: 175.615
• Hs Code.: 2923900090
• European Community (EC) Number: 844-430-4
• DSSTox Substance ID: DTXSID60537564
• Mol file: 1124-40-9.mol

Synonyms:3,4-dihydroxybenzylamine;3,4-dihydroxybenzylamine hydrobromide;3,4-dihydroxybenzylamine hydrochloride

Chemical Property of 4-(Aminomethyl)benzene-1,2-diol hydrochloride

Chemical Property:

• PSA: 66.48000
• LogP: 2.05880
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 175.0400063
• Heavy Atom Count: 11
• Complexity: 108

Purity/Quality:

98%,99%, ^*data from raw suppliers

4-(Aminomethyl)benzene-1,2-diolhydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1CN)O)O.Cl
• Uses: 1,?2-?Benzenediol, 4-?(aminomethyl)?-?, Hydrochloride (1:1) has found use for creating high strength benzoxazine structural adhesives.

Technology Process of 4-(Aminomethyl)benzene-1,2-diol hydrochloride

There total 4 articles about 4-(Aminomethyl)benzene-1,2-diol 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: 89.0%

(E)-3,4-dihydroxybenzaldehyde oxime (3343-59-7) → 3,4-dihydroxybenzylamine hydrochloride (1124-40-9)

Guidance literature:

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 12h;

DOI:10.1002/anie.201906008

Reference yield:

3,4-dihydroxybenzaldehyde oxime (3343-59-7) → 3,4-dihydroxybenzylamine hydrochloride (1124-40-9)

Guidance literature:

With hydrogenchloride; hydrogen; palladium 10% on activated carbon; In ethanol; water; under 760.051 Torr;

Reference yield:

N-methoxy-3,4-dihydroxybenzaldimine → 3,4-dihydroxybenzylamine hydrochloride (1124-40-9)

Guidance literature:

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃;

DOI:10.1021/jm801026e

upstream raw materials:

3,4-dihydroxybenzaldehyde

3,4-dihydroxybenzaldehyde oxime

(E)-3,4-dihydroxybenzaldehyde oxime

Downstream raw materials:

N-(3,4-dihydroxybenzyl)-N'-hexylthiourea

[1S-(1α,2β,3β,4α)]-4-[7-(Butylamino)-5-(propylthio)-3H-1,2,3-triazolo[4,5-d]pyrimidin-3-yl]-2,3-dihydroxy-N-[(3,4-dihydroxyphenyl)methyl]-cyclopentanecarboxamide

5-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-2,4-dihydroxy-benzoic acid amide

3-adamantan-1-yl-N-(3,4-dihydroxybenzyl)-4-methoxy-benzoic acid amide

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