(3-(Benzyloxy)phenyl)methanamine hydrochloride

Base Information

• Chemical Name: (3-(Benzyloxy)phenyl)methanamine hydrochloride
• CAS No.: 104566-41-8
• Molecular Formula: C14H16ClNO
• Molecular Weight: 249.74
• European Community (EC) Number: 829-900-9
• Mol file: 104566-41-8.mol

Synonyms:(3-(Benzyloxy)phenyl)methanamine hydrochloride;104566-41-8;[3-(benzyloxy)phenyl]methanamine hydrochloride;(3-(BENZYLOXY)PHENYL)METHANAMINE HCL;(3-phenylmethoxyphenyl)methanamine;hydrochloride;[3-(Benzyloxy)benzyl]amine hydrochloride;(3-(Benzyloxy)phenyl)methanaminehydrochloride;3-benzyloxybenzylamine hydrochloride;SCHEMBL538603;3-benzyloxybenzylaminehydrochloride;OOQQYQQLMPJNJB-UHFFFAOYSA-N;MFCD15732122;AKOS000283406;DS-4742;DB-145786;CS-0156166;EN300-211530;O10063;1-[3-(benzyloxy)phenyl]methanamine hydrochloride;A922026;Z2092369091

Chemical Property of (3-(Benzyloxy)phenyl)methanamine hydrochloride

Chemical Property:

• PSA: 35.25000
• LogP: 4.22660
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 249.0920418
• Heavy Atom Count: 17
• Complexity: 189

Purity/Quality:

97% ^*data from raw suppliers

(3-(Benzyloxy)phenyl)methanaminehydrochloride 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)COC2=CC=CC(=C2)CN.Cl

Technology Process of (3-(Benzyloxy)phenyl)methanamine hydrochloride

There total 4 articles about (3-(Benzyloxy)phenyl)methanamine 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: 79.0%

[3-(benzyloxy)phenyl]methanamine (104566-43-0) → 3-(benzyloxy)benzylamine hydrochloride (104566-41-8)

Guidance literature:

With hydrogenchloride; In dichloromethane; at 20 ℃; for 1h;

Reference yield: 40.0%

diethyl ether (60-29-7,927820-24-4) + 3-Benzyloxybenzaldehyde (1700-37-4) → 3-(benzyloxy)benzylamine hydrochloride (104566-41-8)

Guidance literature:

With sodium borohydrid; In ethanol; ammonia; water;

Reference yield:

4-cyano-2-benzyloxypyridine (61147-43-1) → 3-(benzyloxy)benzylamine hydrochloride (104566-41-8)

Guidance literature:

4-cyano-2-benzyloxypyridine; With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 4.16667h;

With water; ethyl acetate; In diethyl ether;

With hydrogenchloride; In diethyl ether; water;

upstream raw materials:

4-cyano-2-benzyloxypyridine

diethyl ether

3-Benzyloxybenzaldehyde

N-methoxylamine hydrochloride

Downstream raw materials:

4-Chloro-5-(3-benzyloxybenzylamino)-2-i-propyl-3-(2H)pyridazinone

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