2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide

Base Information

Chemical Name:2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide
CAS No.:104155-72-8
Molecular Formula:C₁₈H₁₄BrNO
Molecular Weight:340.219
Hs Code.:
DSSTox Substance ID:DTXSID90546528
Wikidata:Q82424391
Mol file:104155-72-8.mol

Synonyms:104155-72-8;2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide;DTXSID90546528

Suppliers and Price of 2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:339.02588
Heavy Atom Count:21
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N(C2=CC=CC3=CC=CC=C32)C(=O)CBr

Technology Process of 2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide

There total 1 articles about 2-Bromo-N-(naphthalen-1-yl)-N-phenylacetamide 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: 74.0%

: 90-30-2
N-phenyl-1-naphthylamine

: 598-21-0
2-Bromoacetyl bromide

: 104155-72-8
2-Brom-N-(1-naphthyl)acetanilid

Guidance literature:: With pyridine; In toluene; for 12h; Ambient temperature;

Reference yield: 60.0%

: 603-35-0
triphenylphosphine

: 104155-72-8
2-Brom-N-(1-naphthyl)acetanilid

: 104155-74-0
<<(1-Naphthyl)phenylcarbamoyl>methyl>triphenylphosphonium-bromid

Guidance literature:: In toluene; for 16h; Ambient temperature;

Reference yield:

: 104155-72-8
2-Brom-N-(1-naphthyl)acetanilid

: 104155-80-8
N-(1-Naphthyl)-N-phenyl-2,3-butadienamid

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / toluene / 16 h / Ambient temperature

2: 81 percent / (C₂H₅)3N / 3 h / Ambient temperature

3: 49 percent / CH₂Cl₂ / 1 h / Ambient temperature

With triethylamine; In dichloromethane; toluene;