(2-Phenoxyphenyl)methanamine

Base Information

• Chemical Name: (2-Phenoxyphenyl)methanamine
• CAS No.: 107624-14-6
• Molecular Formula: C13H13NO
• Molecular Weight: 199.252
• Hs Code.: 2922299090
• European Community (EC) Number: 692-968-1
• ChEMBL ID: CHEMBL5195142
• DSSTox Substance ID: DTXSID20590019
• Wikidata: Q82483669
• Mol file: 107624-14-6.mol

Synonyms:(2-phenoxyphenyl)methanamine;107624-14-6;2-phenoxy-benzylamine;1-(2-phenoxyphenyl)methanamine;Benzenemethanamine, 2-phenoxy-;SCHEMBL1196716;CHEMBL5195142;DTXSID20590019;STL414992;AKOS000261451;CCG-356690;CS-0416095;EN300-59205;C77749;SLY

Chemical Property of (2-Phenoxyphenyl)methanamine

Chemical Property:

• PSA: 35.25000
• LogP: 3.63790
• Storage Temp.: 2-8°C
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 199.099714038
• Heavy Atom Count: 15
• Complexity: 177

Purity/Quality:

98%min ^*data from raw suppliers

(2-Phenoxyphenyl)methanamine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)OC2=CC=CC=C2CN

Technology Process of (2-Phenoxyphenyl)methanamine

There total 7 articles about (2-Phenoxyphenyl)methanamine 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-phenoxyphenyl)methanamine (107624-14-6)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield: 83.0%

C13H11N3O → (2-phenoxyphenyl)methanamine (107624-14-6)

Guidance literature:

With water; In tetrahydrofuran; at 75 ℃; for 2h;

Reference yield:

o-phenoxybenzonitrile (6476-32-0) → (2-phenoxyphenyl)methanamine (107624-14-6)

Guidance literature:

With lithium aluminium tetrahydride;

DOI:10.1021/jm00236a006

upstream raw materials:

hexamethylenetetramine

2-bromomethylphenyl phenyl ether

o-phenoxybenzonitrile

1-methyl-2-phenoxybenzene

Downstream raw materials:

2-[4-methoxy-3-(2-phenoxy-benzylcarbamoyl)-benzyl]-butyric acid ethyl ester

(2-phenoxybenzyl)amine hydrochloride