Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)-

Base Information

• Chemical Name: Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)-
• CAS No.: 61692-96-4
• Molecular Formula: C15H11Cl
• Molecular Weight: 226.705
• DSSTox Substance ID: DTXSID80439278
• Nikkaji Number: J504.728E
• Mol file: 61692-96-4.mol

Synonyms:61692-96-4;Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)-;DTXSID80439278;1-Phenyl-3-(4-chlorophenyl)-1,2-propanediene

Chemical Property of Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)-

Chemical Property:

• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 226.0549280
• Heavy Atom Count: 16
• Complexity: 249

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C=C=CC2=CC=C(C=C2)Cl

Technology Process of Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)-

There total 16 articles about Benzene, 1-chloro-4-(3-phenyl-1,2-propadienyl)- 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: 92.0%

p-chlorophenyldiazomethane (19277-54-4) + phenylacetylene (536-74-3) → 1-chloro-4-(3-phenylpropa-1,2-dien-1-yl)benzene (61692-96-4)

Guidance literature:

phenylacetylene; With copper(l) iodide; triethylamine; In 1,4-dioxane; for 0.166667h; Flow reactor;

p-chlorophenyldiazomethane; In 1,4-dioxane; dichloromethane; at 20 ℃; for 0.166667h; Flow reactor;

DOI:10.1002/anie.201501538

Reference yield:

((S)-1-((S)-1-(4-chlorophenyl)-3-phenylprop-2-yn-1-yl)pyrrolidin-2-yl)methanol (1009080-82-3) → C15H11Cl (61692-96-4) + C15H11Cl (61692-96-4)

Guidance literature:

potassium tetrachloroaurate(III); In acetonitrile; at 40 ℃; for 24h; Title compound not separated from byproducts.;

DOI:10.1021/ol702970r

Reference yield:

((S)-1-((S)-1-(4-chlorophenyl)-3-phenylprop-2-yn-1-yl)pyrrolidin-2-yl)methanol (1009080-82-3) → C15H11Cl (61692-96-4) + C15H11Cl (61692-96-4)

Guidance literature:

potassium tetrachloroaurate(III); In acetonitrile; at 40 ℃; for 24h; Title compound not separated from byproducts.;

DOI:10.1021/ol702970r

upstream raw materials:

ethyl N-nitroso-N-<(E)-2-(p-chlorophenyl)-3-phenylcyclopropyl>carbamate

1-chloro-4-(3-phenylprop-2-yn-1-yl)benzene

(E)-1-(4-chlorophenyl)-2-phenylethene

(4-chlorobenzyl)triphenylphosphonium chloride