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1-Naphthalenol, phenylcarbamate

Base Information
  • Chemical Name:1-Naphthalenol, phenylcarbamate
  • CAS No.:38357-69-6
  • Molecular Formula:C17H13NO2
  • Molecular Weight:263.296
  • Hs Code.:2924299090
  • ChEMBL ID:CHEMBL2288451
  • Mol file:38357-69-6.mol
1-Naphthalenol, phenylcarbamate

Synonyms:1-Naphthalenol, phenylcarbamate;38357-69-6;SCHEMBL9230576;CHEMBL2288451;AKOS024437426

Suppliers and Price of 1-Naphthalenol, phenylcarbamate
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 6 raw suppliers
Chemical Property of 1-Naphthalenol, phenylcarbamate
Chemical Property:
  • PSA:38.33000 
  • LogP:4.52370 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:263.094628657
  • Heavy Atom Count:20
  • Complexity:325
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)NC(=O)OC2=CC=CC3=CC=CC=C32
Technology Process of 1-Naphthalenol, phenylcarbamate

There total 6 articles about 1-Naphthalenol, phenylcarbamate 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 sodium azide; In 1,4-dioxane; at 60 ℃; for 12h; under 760.051 Torr;
DOI:10.1002/ejoc.201901140
Guidance literature:
With sodium azide; In 1,4-dioxane; at 60 ℃; for 12h; under 760.051 Torr;
DOI:10.1002/ejoc.201901140
Guidance literature:
Multi-step reaction with 2 steps
1: N.N-dimethyl-aniline; benzene / 5 - 8 °C
2: aqueous sodium carbonate
With sodium carbonate; N,N-dimethyl-aniline; benzene;
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