17714-40-8

Upstream product

• 1138-47-2 trans-1,2-diphenylcyclopropane 
• 5355-61-3 1,3-diphenyl-1,3-propanediol 
• 100-42-5 styrene 
• 100-52-7 benzaldehyde 
• 1138-48-3 cis-1,2-diphenylcyclopropane 

Downstream Products

• 1448460-54-5 (1,4)-diphenylcyclopenta-(2,3)-[6,6]-C₆₀-fullerene 
• 4274-63-9 4-(3-Hydroxy-1,3-diphenyl-propylamino)-benzoic acid methyl ester 
• 4274-54-8 1,3-diphenyl-3-<(4-methoxyphenyl)amino>-1-propanol 
• 4566-59-0 3-(4-Bromo-phenylamino)-1,3-diphenyl-propan-1-ol 
• 13787-96-7 2,3,5-Triphenylisoxazolidine 
• 4566-58-9 1,3-Diphenyl-3-phenylaminopropanol 

Relevant academic research and scientific papers

Thermodynamic control of quantum defects on single-walled carbon nanotubes

Single-walled carbon nanotubes with designed quantum defects are prepared and characterized. The photoluminescence (PL) of the nanotubes can be modified by thermal treatment from 1215-1224 to 1249-1268 nm. Theoretical calculations suggest that the change

Lewis acid mediated reactions of aldehydes with styrene derivatives: Synthesis of 1,3-Dihalo-1,3-diarylpropanes and 3-chloro-1,3-diarylpropanols

The reactions of aryl aldehydes with styrene derivatives, mediated by various boron Lewis acids, were investigated. 1,3-Dihalo-1,3-diarylpropanes were obtained in high yields with boron trihalides, while 3-chloro-1,3- diarylpropanols were obtained in good

A new convenient, efficient, and regioselective synthesis of 1,3-diaryl-1,3-dihalopropanes

Reactions of aryl aldehydes with styrenes in the presence of boron trihalides produce 1,3-diaryl-1,3-dihalopropanes in excellent yields.

Kinetic Study of the Homolytic Brominolysis of 1,2-Diarylcyclopropanes

The rate constants for the photolytic brominolysis of 22 trans-1,2-diarylcyclopropanes in carbon disulfide relative to an internal standard, p-chlorotoluene, have been determined.The products of the brominolysis are 1,3-dibromo-1,3-diarylpropanes.The rate constants range over 5 orders of magnitude, being enhanced by electrondonating substituents on one or both benzene rings.The quantitative size of the substituent effect (ρ) at either involved carbon center is a function of the substituent at the other center.This fact suggests a continuum of transition-state structures with varying degrees of bond breaking and charge separation.