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4-CHLORO-2-ETHYL-1-INDANONE

Base Information Edit
  • Chemical Name:4-CHLORO-2-ETHYL-1-INDANONE
  • CAS No.:1003708-98-2
  • Molecular Formula:C11H11ClO
  • Molecular Weight:194.65744
  • Hs Code.:2914700090
  • Mol file:1003708-98-2.mol
4-CHLORO-2-ETHYL-1-INDANONE

Synonyms:4-chloro-2-ethyl-2,3-dihydroinden-1-one;

Suppliers and Price of 4-CHLORO-2-ETHYL-1-INDANONE
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
  • Crysdot
  • 4-Chloro-2-ethyl-2,3-dihydro-1H-inden-1-one 95+%
  • 1g
  • $ 377.00
  • American Custom Chemicals Corporation
  • 4-CHLORO-2-ETHYL-2,3-DIHYDRO-1H-INDEN-1-ONE 95.00%
  • 5MG
  • $ 502.67
  • Alichem
  • 4-Chloro-2-ethyl-2,3-dihydro-1H-inden-1-one
  • 1g
  • $ 400.00
Total 8 raw suppliers
Chemical Property of 4-CHLORO-2-ETHYL-1-INDANONE Edit
Chemical Property:
  • PSA:17.07000 
  • LogP:3.10500 
  • Storage Temp.:2-8°C 
Purity/Quality:

98%min *data from raw suppliers

4-Chloro-2-ethyl-2,3-dihydro-1H-inden-1-one 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 4-CHLORO-2-ETHYL-1-INDANONE

There total 2 articles about 4-CHLORO-2-ETHYL-1-INDANONE 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 3-methylpyridin-2-ylamine; chlorobis(ethylene)rhodium(I) dimer; water; toluene-4-sulfonic acid; 1,3-bis(2,4,6-trimethylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene; In tetrahydrofuran; at 150 ℃; for 72h; under 5171.62 Torr; chemoselective reaction;
DOI:10.1021/jacs.9b07445
Guidance literature:
Refernces Edit
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