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11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid

Base Information Edit
  • Chemical Name:11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid
  • CAS No.:7065-21-6
  • Molecular Formula:C24H20 Bi2
  • Molecular Weight:726.384
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30414550
  • Mol file:7065-21-6.mol
11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid

Synonyms:7065-21-6;AC1NRHK6;DTXSID30414550

Suppliers and Price of 11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid Edit
Chemical Property:
  • Vapor Pressure:3.82E-18mmHg at 25°C 
  • Boiling Point:642.2°C at 760 mmHg 
  • Flash Point:342.2°C 
  • Density:1.24g/cm3 
  • XLogP3:6.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:16
  • Exact Mass:614.29604831
  • Heavy Atom Count:42
  • Complexity:1160
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCN1C(=C(C(=C(C1=O)C#N)C)C=C2C(=O)N(C(=S)S2)CCCCCCCCCCC(=O)O)N3CCCCCC3
Technology Process of 11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid

There total 26 articles about 11-[5-[[2-(Azepan-1-yl)-1-butyl-5-cyano-4-methyl-6-oxopyridin-3-yl]methylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]undecanoic acid 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:
In tetrahydrofuran; addn. of soln. of Cp2Co to soln. of BiPh2Cl (room temp., dropwise, 5 min), filtration; evapn. to dryness (vac., room temp.), recrystn. (EtOH); elem. anal., IR spectroscopy;
Guidance literature:
In tetrahydrofuran; (N2), added dropwise, cooled at -40°C; filtered, dried in vac., soln. evaporated, diluted with heptane, cooled at -30°C, filtered, dried in vac.; elem. anal., IR;
Guidance literature:
With Na; In ammonia; NH3 (liquid); To a suspn. of Ph2BiI in liquid NH3 sodium sand was added for about 30 min, temp. between -80 and -50°C, inert atm.;; ppt. was filtered, extd. with toluene at room temp., soln. was filtered, evapd., to dryness, recrystd. from hot abs. EtOH; elem. anal.;;
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