N-(2-Bromoethyl)naphthalene-2-carboxamide

Base Information

Chemical Name:N-(2-Bromoethyl)naphthalene-2-carboxamide
CAS No.:82408-26-2
Molecular Formula:C₁₃H₁₂BrNO
Molecular Weight:278.148
Hs Code.:
DSSTox Substance ID:DTXSID50509573
Wikidata:Q82367246

Synonyms:N-(2-Bromoethyl)naphthalene-2-carboxamide;82408-26-2;DTXSID50509573;AKOS008998748

Suppliers and Price of N-(2-Bromoethyl)naphthalene-2-carboxamide

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 N-(2-Bromoethyl)naphthalene-2-carboxamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:277.01023
Heavy Atom Count:16
Complexity:244

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)C(=O)NCCBr

Technology Process of N-(2-Bromoethyl)naphthalene-2-carboxamide

There total 2 articles about N-(2-Bromoethyl)naphthalene-2-carboxamide 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: 91.0%

: 63021-45-4
1-(2-naphthoyl)aziridine

: 10431-96-6
2-(naphthalen-2-yl)-4,5-dihydrooxazole

: 82408-26-2
N-(2-bromoethyl)-2-naphthamide

Guidance literature:: With 1,3,5-trisbromobenzene; In benzene; for 3.33333h; Product distribution; Quantum yield; Mechanism; Ambient temperature; Irradiation; different brominated hydrocarbons, 1,3,5-tribromobenzene concentrations, added photosensitizers, reaction times and solvents; effect of solvent polarity;
DOI:10.1039/P29830001147