1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene

Base Information

• Chemical Name: 1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene
• CAS No.: 120578-04-3
• Molecular Formula: C28H18Cl2N2
• Molecular Weight: 453.37
• DSSTox Substance ID: DTXSID20559782
• Nikkaji Number: J1.644.737D,J1.805.791C
• Wikidata: Q82442625
• Mol file: 120578-04-3.mol

Synonyms:120578-04-3;1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene;7-chloro-2-[(E)-2-[3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]ethenyl]quinoline;SCHEMBL13513030;DTXSID20559782;2,2'-{1,3-Phenylenedi[(E)ethene-2,1-diyl]}bis(7-chloroquinoline);7-CHLORO-2-((E)-2-[3-[(E)-2-(7-CHLORO-2-QUINOLINYL)ETHENYL]PHENYL]ETHENYL)QUINOLINE

Chemical Property of 1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene

Chemical Property:

• PSA: 25.78000
• LogP: 8.43060
• XLogP3: 8.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 452.0847040
• Heavy Atom Count: 32
• Complexity: 610

Purity/Quality:

≥95% ^*data from raw suppliers

7-Chloro-2-[(E)-2-[3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]ethenyl]quinoline ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)C=CC2=NC3=C(C=CC(=C3)Cl)C=C2)C=CC4=NC5=C(C=CC(=C5)Cl)C=C4
• Isomeric SMILES: C1=CC(=CC(=C1)/C=C/C2=NC3=C(C=CC(=C3)Cl)C=C2)/C=C/C4=NC5=C(C=CC(=C5)Cl)C=C4
• Uses: 7-Chloro-2-[(E)-2-[3-[(E)-2-(7-chloroquinolin-2-yl)ethenyl]phenyl]ethenyl]quinoline is a reagent in the synthesis of dithioacetals, which are intermediates in the preparation of potent LTD4 antagonist L-660,711.

Technology Process of 1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene

There total 1 articles about 1,3-Bis[2-(7-chloro-2-quinolyl)vinyl]benzene 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:

Reference yield: 65.45%

2-methyl-7-chloroquinoline (4965-33-7) + Isophthalaldehyde (626-19-7) → (E)-3-[2-(7-chloro-2-quinolinyl)ethenyl]benzaldehyde (120578-03-2) + C28H18Cl2N2 (120578-04-3)

Guidance literature:

With acetic acid; at 100 ℃; Product distribution / selectivity;

upstream raw materials:

2-methyl-7-chloroquinoline

Isophthalaldehyde