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3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)

Base Information Edit
  • Chemical Name:3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)
  • CAS No.:59826-28-7
  • Molecular Formula:C7H10ClNO
  • Molecular Weight:159.615
  • Hs Code.:
  • Mol file:59826-28-7.mol
3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)

Synonyms:3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)

Suppliers and Price of 3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)
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
  • TRC
  • 1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarbonylChloride
  • 250mg
  • $ 475.00
Total 3 raw suppliers
Chemical Property of 3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI) Edit
Chemical Property:
  • Boiling Point:228.1±29.0 °C(Predicted) 
  • PKA:7?+-.0.40(Predicted) 
  • PSA:20.31000 
  • Density:1.182±0.06 g/cm3(Predicted) 
  • LogP:0.95160 
Purity/Quality:

99% *data from raw suppliers

1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarbonylChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarbonyl Chloride is used in the synthesis of 6-substituted-4-(3-bromophenylamino)quinazoline derivatives which functions as irreversible inhibitor of epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor (HER-2) tyrosine kinases.Also, it is an intermediate used in the synthesis of Arecaidine But-2-ynyl Ester Tosylate (A767018), which is a potent, selective mAChR M2 activator.
Technology Process of 3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI)

There total 3 articles about 3-Pyridinecarbonyl chloride, 1,2,5,6-tetrahydro-1-methyl- (9CI) 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: 8.2 g / water / 24 h / Heating
2: thionyl chloride / 2 h / Heating
With thionyl chloride; water; 1: Hydrolysis / 2: Chlorination;
DOI:10.1016/S0968-0896(00)00033-X
Guidance literature:
Multi-step reaction with 3 steps
1: aq. Na2CO3 / pH 10 - 11
2: 8.2 g / water / 24 h / Heating
3: thionyl chloride / 2 h / Heating
With thionyl chloride; water; sodium carbonate; 1: deprotonation / 2: Hydrolysis / 3: Chlorination;
DOI:10.1016/S0968-0896(00)00033-X
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