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2-(1-Naphthalenylcarbonyl)-propanedinitrile

Base Information
  • Chemical Name:2-(1-Naphthalenylcarbonyl)-propanedinitrile
  • CAS No.:1236038-48-4
  • Molecular Formula:C14H8N2O
  • Molecular Weight:220.23
  • Hs Code.:
  • Mol file:1236038-48-4.mol
2-(1-Naphthalenylcarbonyl)-propanedinitrile

Synonyms:2-(1-Naphthalenylcarbonyl)-propanedinitrile

Suppliers and Price of 2-(1-Naphthalenylcarbonyl)-propanedinitrile
Supply Marketing:
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
  • 2-(1-Naphthalenylcarbonyl)propanedinitrile
  • 50mg
  • $ 305.00
  • Matrix Scientific
  • 2-(1-Naphthoyl)malononitrile 97%
  • 25g
  • $ 3240.00
  • Matrix Scientific
  • 2-(1-Naphthoyl)malononitrile 97%
  • 5g
  • $ 1080.00
  • Crysdot
  • 2-(1-Naphthoyl)malononitrile 95+%
  • 5g
  • $ 1072.00
  • Chemenu
  • 2-(1-Naphthoyl)malononitrile 95%
  • 5g
  • $ 1010.00
  • American Custom Chemicals Corporation
  • 2-(1-NAPHTHALENYLCARBONYL)PROPANEDINITRILE 95.00%
  • 250MG
  • $ 255.15
Total 7 raw suppliers
Chemical Property of 2-(1-Naphthalenylcarbonyl)-propanedinitrile
Chemical Property:
  • PSA:64.65000 
  • LogP:2.68586 
  • Solubility.:Chloroform, Ethyl Acetate 
Purity/Quality:

≥95% *data from raw suppliers

2-(1-Naphthalenylcarbonyl)propanedinitrile *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 2-(1-Naphthalenylcarbonyl)-propanedinitrile is used in the preparation of inhibitors that target calcium-dependent protein kinases in C. parvum and T. gondii parazites.
Technology Process of 2-(1-Naphthalenylcarbonyl)-propanedinitrile

There total 2 articles about 2-(1-Naphthalenylcarbonyl)-propanedinitrile 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 sodium hydride; In tetrahydrofuran; paraffin oil (nujol); at 5 - 10 ℃; for 3h;
Guidance literature:
Multi-step reaction with 2 steps
1: oxalyl dichloride / N,N-dimethyl-formamide; hexane / 1 h / 20 °C
2: sodium hydride / tetrahydrofuran / 1 h / 20 °C
With oxalyl dichloride; sodium hydride; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jm4001314
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydrogencarbonate / water; 1,4-dioxane / 1 h / Reflux
2: ethanol / 1 h / Reflux
With sodium hydrogencarbonate; In 1,4-dioxane; ethanol; water;
DOI:10.1021/jm4001314
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