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1H-Pyrrolo[3,2-b]pyridine-5-methanol

Base Information Edit
  • Chemical Name:1H-Pyrrolo[3,2-b]pyridine-5-methanol
  • CAS No.:1346569-67-2
  • Molecular Formula:C8H8N2O
  • Molecular Weight:148.16200
  • Hs Code.:
  • Mol file:1346569-67-2.mol
1H-Pyrrolo[3,2-b]pyridine-5-methanol

Synonyms:

Suppliers and Price of 1H-Pyrrolo[3,2-b]pyridine-5-methanol
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
  • Alichem
  • (1H-Pyrrolo[3,2-b]pyridin-5-yl)methanol
  • 25g
  • $ 5382.78
  • Alichem
  • (1H-Pyrrolo[3,2-b]pyridin-5-yl)methanol
  • 10g
  • $ 2814.00
  • Alichem
  • (1H-Pyrrolo[3,2-b]pyridin-5-yl)methanol
  • 5g
  • $ 2190.90
Total 1 raw suppliers
Chemical Property of 1H-Pyrrolo[3,2-b]pyridine-5-methanol Edit
Chemical Property:
  • PSA:48.91000 
  • LogP:1.05520 
Purity/Quality:

98% *data from raw suppliers

(1H-Pyrrolo[3,2-b]pyridin-5-yl)methanol *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1H-Pyrrolo[3,2-b]pyridine-5-methanol

There total 4 articles about 1H-Pyrrolo[3,2-b]pyridine-5-methanol 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 lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.5b01240
Guidance literature:
Multi-step reaction with 4 steps
1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / 22 - 26 °C
2: pyridine / dichloromethane / 2 h / 0 - 26 °C
3: tetrabutyl ammonium fluoride / tetrahydrofuran / 8 h / Reflux
4: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C
With pyridine; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In tetrahydrofuran; dichloromethane; 1: Sonogashira Coupling;
Guidance literature:
Multi-step reaction with 3 steps
1: pyridine / dichloromethane / 2 h / 0 - 26 °C
2: tetrabutyl ammonium fluoride / tetrahydrofuran / 8 h / Reflux
3: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C
With pyridine; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane;
Refernces Edit
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