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ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-

Base Information
  • Chemical Name:ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-
  • CAS No.:3289-00-7
  • Molecular Formula:C12H17NO2
  • Molecular Weight:0
  • Hs Code.:2924299090
  • DSSTox Substance ID:DTXSID50186540
  • Nikkaji Number:J55.165A
  • Wikidata:Q83057857
  • Mol file:3289-00-7.mol
ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-

Synonyms:2-(p-tert-Butylphenyl)acetohydroxamic acid;3289-00-7;BRN 2213421;ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-;SCHEMBL15581376;DTXSID50186540

Suppliers and Price of ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-
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
  • American Custom Chemicals Corporation
  • 2-(PARA-TERT-BUTYLPHENYL)ACETOHYDROXAMIC ACID 95.00%
  • 5MG
  • $ 505.14
Total 4 raw suppliers
Chemical Property of ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-
Chemical Property:
  • PSA:52.82000 
  • Density:1.077g/cm3 
  • LogP:2.87230 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:207.125928785
  • Heavy Atom Count:15
  • Complexity:212
Purity/Quality:

95% *data from raw suppliers

2-(PARA-TERT-BUTYLPHENYL)ACETOHYDROXAMIC ACID 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)C1=CC=C(C=C1)CC(=O)NO
Technology Process of ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)-

There total 4 articles about ACETOHYDROXAMIC ACID, 2-(p-tert-BUTYLPHENYL)- 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:
4-t-butylphenylacetic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 23 ℃; for 1h; Inert atmosphere;
In tetrahydrofuran; at 23 ℃; for 12h; Inert atmosphere;
DOI:10.1002/ejoc.202100113
Guidance literature:
Multi-step reaction with 2 steps
1: (i) HCl, (ii) /BRN= 3587243/, DMSO, (iii) /BRN= 1718733/, H2SO4
2: NH2OH*HCl, NaOMe / methanol / Heating
With hydroxylamine hydrochloride; sodium methylate; In methanol;
Guidance literature:
With hydroxylamine hydrochloride; sodium methylate; In methanol; Heating;
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