N-2-Naphthylbenzamide

Base Information

Chemical Name:N-2-Naphthylbenzamide
CAS No.:18271-22-2
Molecular Formula:C17H13 N O
Molecular Weight:247.296
Hs Code.:2924299090
European Community (EC) Number:242-151-7
NSC Number:99837
DSSTox Substance ID:DTXSID20171322
Nikkaji Number:J266.089J
Wikidata:Q83041397
Mol file:18271-22-2.mol

Synonyms:N-2-Naphthylbenzamide;18271-22-2;N-(2-Naphthyl)benzamide;N-naphthalen-2-ylbenzamide;N-(naphthalen-2-yl)benzamide;Benzamide, N-2-naphthalenyl-;EINECS 242-151-7;NSC99837;N-2-Naphthalenylbenzamide;N-Benzoyl-2-naphthylamin;NCIOpen2_007223;N-(2-Naphthyl)benzamide #;SCHEMBL2229842;DTXSID20171322;NSC 99837;NSC-99837;STL257150;AKOS002985092;CS-0236082;AE-641/02441037;EN300-16795594

Suppliers and Price of N-2-Naphthylbenzamide

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

Aronis compounds
N-2-naphthylbenzamide
5mg
$ 15.00

American Custom Chemicals Corporation
N-2-NAPHTHYLBENZAMIDE 95.00%
5MG
$ 495.21

Total 7 raw suppliers

Chemical Property of N-2-Naphthylbenzamide

Chemical Property:

Vapor Pressure:5.31E-05mmHg at 25°C
Boiling Point:347.6°Cat760mmHg
Flash Point:210.2°C
PSA：29.10000
Density:1.221g/cm³
LogP:4.16510
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:247.099714038
Heavy Atom Count:19
Complexity:308

Purity/Quality:

99% ^*data from raw suppliers

N-2-naphthylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC2=CC3=CC=CC=C3C=C2

Technology Process of N-2-Naphthylbenzamide

There total 37 articles about N-2-Naphthylbenzamide 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: 99.0%

: 93-97-0
benzoic acid anhydride

: 91-59-8
naphthalen-2-ylamine

: 18271-22-2
N-(naphthalen-2-yl)benzamide

Guidance literature:: benzoic acid anhydride; With molybdenium(VI) dioxodichloride; In dichloromethane; at 20 ℃; for 0.5h;

naphthalen-2-ylamine; In dichloromethane; at 20 ℃; for 50h;
DOI:10.1021/jo048363v

Reference yield: 97.0%

: 451-40-1
phenyl benzyl ketone

: 91-59-8
naphthalen-2-ylamine

: 18271-22-2
N-(naphthalen-2-yl)benzamide

: 100-52-7
benzaldehyde

Guidance literature:: With 1,10-Phenanthroline; copper(II) chloride dihydrate; oxygen; In acetonitrile; for 24h; under 760.051 Torr; Reflux;
DOI:10.1021/acs.joc.5b01670