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N-Hydroxy-N-(naphthalen-1-yl)acetamide

Base Information Edit
  • Chemical Name:N-Hydroxy-N-(naphthalen-1-yl)acetamide
  • CAS No.:38105-20-3
  • Molecular Formula:C12H11NO2
  • Molecular Weight:201.225
  • Hs Code.:
  • ChEMBL ID:CHEMBL314719
  • DSSTox Substance ID:DTXSID60500930
  • Nikkaji Number:J2.457.595K
  • Wikidata:Q82352973
  • Mol file:38105-20-3.mol
N-Hydroxy-N-(naphthalen-1-yl)acetamide

Synonyms:38105-20-3;N-Hydroxy-N-(naphthalen-1-yl)acetamide;CHEMBL314719;SCHEMBL10958989;DTXSID60500930

Suppliers and Price of N-Hydroxy-N-(naphthalen-1-yl)acetamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of N-Hydroxy-N-(naphthalen-1-yl)acetamide Edit
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:201.078978594
  • Heavy Atom Count:15
  • Complexity:242
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)N(C1=CC=CC2=CC=CC=C21)O
Technology Process of N-Hydroxy-N-(naphthalen-1-yl)acetamide

There total 1 articles about N-Hydroxy-N-(naphthalen-1-yl)acetamide 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 water; In acetone; at 40 ℃; Product distribution; Rate constant; solvolysis at pH = 5-10 values and an ionic strength of 0.25 M (maintained by NaClO4);
DOI:10.1039/c39850000555
Guidance literature:
With Phenylselenyl bromide; In 1,4-dioxane; at 23 ℃; for 12h;
DOI:10.1002/anie.202100801
upstream raw materials:

N-Acetoxy-1-N-acetylaminonaphtalene

Downstream raw materials:

N-(4-hydroxy-1-naphthalenyl)acetamide

Refernces Edit
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