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N-(4-Methoxyphenyl)pivalamide

Base Information
  • Chemical Name:N-(4-Methoxyphenyl)pivalamide
  • CAS No.:56619-94-4
  • Molecular Formula:C12H17NO2
  • Molecular Weight:207.272
  • Hs Code.:2924299090
N-(4-Methoxyphenyl)pivalamide

Synonyms:4-methoxyphenyl pivalamide;Pivalinsaeure-<4-methoxy-anilid>N-pivaloyl-p-anisidine;

Suppliers and Price of N-(4-Methoxyphenyl)pivalamide
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
  • Sigma-Aldrich
  • 2,2-DIMETHYL-4'-METHOXYPROPIONANILIDE Aldrich
  • 100mg
  • $ 57.00
Total 3 raw suppliers
Chemical Property of N-(4-Methoxyphenyl)pivalamide
Chemical Property:
  • PSA:38.33000 
  • LogP:2.75280 
Purity/Quality:

99% *data from raw suppliers

2,2-DIMETHYL-4'-METHOXYPROPIONANILIDE Aldrich *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of N-(4-Methoxyphenyl)pivalamide

There total 15 articles about N-(4-Methoxyphenyl)pivalamide 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 iron(III)-acetylacetonate; In isopropyl alcohol; at 83 ℃; for 24h; Microwave irradiation;
DOI:10.1021/acs.orglett.6b02247
Guidance literature:
With tri(sec-butyl)borane; (DiMeIHeptCl)Pd(cinammyl)Cl; caesium carbonate; In toluene; for 24h; Inert atmosphere; Sealed tube; Schlenk technique; Heating;
DOI:10.1021/jacs.7b09488
Guidance literature:
With sulphuric acid immobilized on silica gel; In neat (no solvent); at 70 ℃; for 7h; Green chemistry;
DOI:10.1039/c4ra16571c
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