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4-isopropylbutyrophenone

Base Information Edit
  • Chemical Name:4-isopropylbutyrophenone
  • CAS No.:78575-06-1
  • Molecular Formula:C13H18 O
  • Molecular Weight:190.28142
  • Hs Code.:
  • Mol file:78575-06-1.mol
4-isopropylbutyrophenone

Synonyms:Butyrophenone,4'-isopropyl- (6CI)

Suppliers and Price of 4-isopropylbutyrophenone
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
  • Packaging
  • price
  • Rieke Metals
  • 1-(4-Isopropyl-phenyl)-butan-1-one
  • 5g
  • $ 1328.00
  • Rieke Metals
  • 1-(4-Isopropyl-phenyl)-butan-1-one
  • 1g
  • $ 527.00
  • American Custom Chemicals Corporation
  • 1-(4-ISOPROPYLPHENYL)BUTAN-1-ONE 95.00%
  • 5MG
  • $ 496.42
Total 5 raw suppliers
Chemical Property of 4-isopropylbutyrophenone Edit
Chemical Property:
  • PSA:17.07000 
  • LogP:3.69560 
Purity/Quality:

98% *data from raw suppliers

1-(4-Isopropyl-phenyl)-butan-1-one *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-isopropylbutyrophenone

There total 2 articles about 4-isopropylbutyrophenone 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 aluminum (III) chloride; In dichloromethane; at 0 ℃; for 2h; Sealed tube; Inert atmosphere;
DOI:10.3987/COM-20-14321
Guidance literature:
With aluminium trichloride; In 1,2-dichloro-ethane; at 20 - 25 ℃; for 0.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate; hydroxylamine hydrochloride / methanol / 16 h / 20 °C / Inert atmosphere
2: diphenylphosphoranyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene / 16 h / 120 °C / Inert atmosphere
With diphenylphosphoranyl azide; hydroxylamine hydrochloride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; toluene;
DOI:10.3987/COM-20-14321
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