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acetaldehyde compound with thieno[2,3-b]pyridine (1:1)

Base Information Edit
  • Chemical Name:acetaldehyde compound with thieno[2,3-b]pyridine (1:1)
  • CAS No.:89723-19-3
  • Molecular Formula:C9H7NOS
  • Molecular Weight:177.227
  • Hs Code.:
  • Mol file:89723-19-3.mol
acetaldehyde compound with thieno[2,3-b]pyridine (1:1)

Synonyms:ETHANONE, 1-THIENO[2,3-B]PYRIDIN-6-YL-;Thieno[2,3-b]pyridine, ethanone deriv.;

Suppliers and Price of acetaldehyde compound with thieno[2,3-b]pyridine (1:1)
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
  • AccelPharmtech
  • 1-thieno[2,3-b]pyridin-6-yl-Ethanone 97.00%
  • 25G
  • $ 6000.00
  • AccelPharmtech
  • 1-thieno[2,3-b]pyridin-6-yl-Ethanone 97.00%
  • 5G
  • $ 3230.00
  • AccelPharmtech
  • 1-thieno[2,3-b]pyridin-6-yl-Ethanone 97.00%
  • 1G
  • $ 1890.00
Total 0 raw suppliers
Chemical Property of acetaldehyde compound with thieno[2,3-b]pyridine (1:1) Edit
Chemical Property:
  • PSA:58.20000 
  • LogP:2.49890 
Purity/Quality:

1-thieno[2,3-b]pyridin-6-yl-Ethanone 97.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of acetaldehyde compound with thieno[2,3-b]pyridine (1:1)

There total 5 articles about acetaldehyde compound with thieno[2,3-b]pyridine (1:1) 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:
Multi-step reaction with 2 steps
1: 36 percent / triethylamine / CHCl3 / 12 h / Heating
2: boron trifluoride etherate / 48 h / Heating
With boron trifluoride diethyl etherate; triethylamine; In chloroform;
Refernces Edit
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