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propyl N-naphthalen-1-ylcarbamate

Base Information
  • Chemical Name:propyl N-naphthalen-1-ylcarbamate
  • CAS No.:25216-27-7
  • Molecular Formula:C14H15NO2
  • Molecular Weight:229.27
  • Hs Code.:2924299090
  • NSC Number:190586
  • DSSTox Substance ID:DTXSID60948070
  • Wikidata:Q82925862
  • Mol file:25216-27-7.mol
propyl N-naphthalen-1-ylcarbamate

Synonyms:propyl N-naphthalen-1-ylcarbamate;propyl N-(naphthalen-1-yl)carbamate;NSC190586;propyl 1-naphthylcarbamate;Propyl 1-naphthalenylcarbamate;SCHEMBL10959203;DTXSID60948070;FFLMQABWXVOTKQ-UHFFFAOYSA-N;AKOS002937060;NSC-190586;Carbamic acid, 1-naphthyl-, propyl ester

Suppliers and Price of propyl N-naphthalen-1-ylcarbamate
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
  • Matrix Scientific
  • 1-Naphthyl N-propylcarbamate
  • 10g
  • $ 100.00
  • AHH
  • 1-NaphthylN-Propylcarbamate 98%
  • 25g
  • $ 310.00
Total 9 raw suppliers
Chemical Property of propyl N-naphthalen-1-ylcarbamate
Chemical Property:
  • Vapor Pressure:0.000151mmHg at 25°C 
  • Melting Point:72 °C 
  • Boiling Point:331.9°Cat760mmHg 
  • PKA:13.86±0.30(Predicted) 
  • Flash Point:154.5°C 
  • PSA:38.33000 
  • Density:1.169g/cm3 
  • LogP:3.72910 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:229.110278721
  • Heavy Atom Count:17
  • Complexity:255
Purity/Quality:

97% *data from raw suppliers

1-Naphthyl N-propylcarbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCOC(=O)NC1=CC=CC2=CC=CC=C21
Technology Process of propyl N-naphthalen-1-ylcarbamate

There total 10 articles about propyl N-naphthalen-1-ylcarbamate 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:
Guidance literature:
With choline chloride * 2ZnCl2; at 20 ℃; for 2h; under 760.051 Torr; Green chemistry;
DOI:10.1039/c9nj02810b
Guidance literature:
With C32H52N2O8PdSi2; sodium t-butanolate; In toluene; at 100 ℃; for 3h;
DOI:10.1039/c6ra17268g
Guidance literature:
With sodium azide; In 1,4-dioxane; at 60 ℃; for 12h; under 760.051 Torr;
DOI:10.1002/ejoc.201901140
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