N-[2-(Aminomethyl)phenyl]acetamide

Base Information

Chemical Name:N-[2-(Aminomethyl)phenyl]acetamide
CAS No.:117995-02-5
Molecular Formula:C₉H₁₂N₂O
Molecular Weight:164.207
Hs Code.:
ChEMBL ID:CHEMBL4548721
DSSTox Substance ID:DTXSID40588170
Nikkaji Number:J1.117.689E
Wikidata:Q82480681
Mol file:117995-02-5.mol

Synonyms:N-[2-(Aminomethyl)phenyl]acetamide;117995-02-5;N-(2-(Aminomethyl)phenyl)acetamide;SCHEMBL8631475;CHEMBL4548721;DTXSID40588170;AKOS002433965;MCULE-3063490873;DB-188234;EN300-147165

Suppliers and Price of N-[2-(Aminomethyl)phenyl]acetamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-[2-(Aminomethyl)phenyl]acetamide

Chemical Property:

XLogP3:-0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:164.094963011
Heavy Atom Count:12
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC=C1CN

Technology Process of N-[2-(Aminomethyl)phenyl]acetamide

There total 2 articles about N-[2-(Aminomethyl)phenyl]acetamide 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:

: 98952-93-3
2-acetylamino-benzaldehyde-oxime

: 117995-02-5
acetic acid-(2-aminomethyl-anilide)

Guidance literature:: With sodium amalgam; ethanol; acetic acid;

Reference yield:

: 13493-47-5
N-(2-formylphenyl)acetamide

: 117995-02-5
acetic acid-(2-aminomethyl-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: alcohol; water; sodium hydroxide; hydroxylamine hydrochloride

2: glacial acetic acid; alcohol; sodium amalgam

With sodium hydroxide; sodium amalgam; ethanol; hydroxylamine hydrochloride; water; acetic acid;