93652-37-0

Basic information

• Product Name: 4-phenyl-3-butenyl para-toluenesulfonate
• CAS NO: 93652-37-0
• Molecular Weight: 302.394
• Mol File: 93652-37-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-phenyl-3-butenyl para-toluenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-3-butenyl para-toluenesulfonate(93652-37-0)
• EPA Substance Registry System: 4-phenyl-3-butenyl para-toluenesulfonate(93652-37-0)

Safety Data

• Hazardous Substances Data: 93652-37-0(Hazardous Substances Data)

Upstream product

• 10229-11-5 4-phenyl-but-3-yn-1-ol 
• 100-42-5 styrene 
• 778-29-0 but-3-enyl 4-methylbenzenesulfonate 
• 91083-82-8 (E)-methyl 4-phenylbut-3-enoate 
• 2243-53-0 trans-styrylacetic acid 
• 937-58-6 (3E)-4-phenyl-3-buten-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 5558-08-7 α-methoxybenzylcyclopropane 
• 57051-04-4 1-Phenyl--methylether 
• 20473-78-3 acetic acid-(4-phenyl-but-3-enyl ester) 
• 1384458-59-6 ((1E,4E)-3-methylocta-1,4-dien-1-yl)benzene 
• 1384458-56-3 (E)-3-(4-phenylbut-3-en-2-yl)aniline 
• 1104996-95-3 (E)-1-chloro-4-(4-phenylbut-3-en-2-yl)benzene 
• 1384458-55-2 (E)-1-(4-phenylbut-3-en-2-yl)-4-(trifluoromethyl)benzene 
• 1236889-29-4 (E)-1-methyl-2-(4-phenylbut-3-en-2-yl)benzene 
• 886-65-7 trans,trans-1,4-Diphenyl-1,3-butadiene 
• 1384458-60-9 ((1E,4E)-3-methylpenta-1,4-diene-1,5-diyl)dibenzene 
• 1236889-34-1 (E)-methyl 4-(4-phenylbut-3-en-2-yl)benzoate 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 27066-35-9 (E)-1,4-diphenylbut-1-ene 
• 7302-00-3 (E)-1,3-diphenyl-1-butene 

Relevant articles and documents

Acid-Catalyzed O-Glycosylation with Stable Thioglycoside Donors

Two classes of thioglycoside, 4-(4-methoxyphenyl)-3-butenylthioglycosides (MBTGs) and 4-(4-methoxyphenyl)-4-pentenylthioglycosides (MPTGs), undergo acid-catalyzed O-glycosylations with a range of sugar and nonsugar alcohols at 25 °C. Electron density at t

A mechanistic alternative for the intramolecular hydroboration of homoallylic amine and phosphine borane complexes

Intramolecular hydroboration is demonstrated starting from homoallylic amine boranes upon activation by iodine. The process involves a B-iodoborane complex as the intermediate and may occur via internal displacement of iodide by the alkene to generate a cationic borane-alkene π-complex on the way to hydroboration products. The reaction can be carried out using a catalytic amount of iodine. Copyright

Intramolecular N-(Acyloxy)iminium Ion-Alkyne Cycloadditions. A New Route to Bicyclic α-Amino Ketones

The intramolecular cyclocondensation of 15 cyclic N-(acyloxy)iminium cations containing tethered alkyne and alkene nucleophiles is reported (eqs 5 and 6).This route to heterotricyclic systems was specifically demonstrated with substrates in which the hete