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2-(Pyridin-3-yl)ethane-1-thiol

Base Information Edit
  • Chemical Name:2-(Pyridin-3-yl)ethane-1-thiol
  • CAS No.:556825-56-0
  • Molecular Formula:C7H9NS
  • Molecular Weight:139.22
  • Hs Code.:2933399990
  • DSSTox Substance ID:DTXSID90553459
  • Wikidata:Q82434044
  • Mol file:556825-56-0.mol
2-(Pyridin-3-yl)ethane-1-thiol

Synonyms:556825-56-0;2-(Pyridin-3-yl)ethane-1-thiol;2-(PYRIDIN-3-YL)ETHANETHIOL;2-pyridin-3-ylethanethiol;3-Pyridineethanethiol(9CI);3-Pyridineethanethiol;SCHEMBL177997;DTXSID90553459;AKOS006306912;CS-0356157;F18092;EN300-1858493

Suppliers and Price of 2-(Pyridin-3-yl)ethane-1-thiol
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
  • SynQuest Laboratories
  • 2-(Pyridin-3-yl)ethane-1-thiol 98%
  • 250 mg
  • $ 960.00
Total 5 raw suppliers
Chemical Property of 2-(Pyridin-3-yl)ethane-1-thiol Edit
Chemical Property:
  • PSA:51.69000 
  • LogP:1.55390 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:139.04557046
  • Heavy Atom Count:9
  • Complexity:75.3
Purity/Quality:

98%min *data from raw suppliers

2-(Pyridin-3-yl)ethane-1-thiol 98% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CN=C1)CCS
Technology Process of 2-(Pyridin-3-yl)ethane-1-thiol

There total 5 articles about 2-(Pyridin-3-yl)ethane-1-thiol 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:
3-pyridylethyl thioacetate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 60 ℃; for 3h; Inert atmosphere; Cooling with ice;
With water; acetic acid; In tetrahydrofuran; Cooling with ice;
With sodium hydrogencarbonate; In tetrahydrofuran; water; ethyl acetate;
Guidance literature:
Multi-step reaction with 2 steps
1.1: ethanol; water / 4 h / Inert atmosphere; Reflux
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 60 °C / Inert atmosphere; Cooling with ice
2.2: Cooling with ice
With lithium aluminium tetrahydride; In tetrahydrofuran; ethanol; water;
Guidance literature:
Multi-step reaction with 3 steps
1.1: thionyl chloride / chloroform / 3 h / 20 °C / Inert atmosphere
2.1: ethanol; water / 4 h / Inert atmosphere; Reflux
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 60 °C / Inert atmosphere; Cooling with ice
3.2: Cooling with ice
With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; ethanol; chloroform; water;
Refernces Edit
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