462637-32-7

Basic information

• Product Name: Benzoic acid, 4-(1-hexynyl)-, methyl ester
• CAS NO: 462637-32-7
• Molecular Formula: C14H16O2
• Molecular Weight: 216.28
• Mol File: 462637-32-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(1-hexynyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(1-hexynyl)-, methyl ester(462637-32-7)
• EPA Substance Registry System: Benzoic acid, 4-(1-hexynyl)-, methyl ester(462637-32-7)

Safety Data

• Hazardous Substances Data: 462637-32-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 693-02-7 hex-1-yne 
• 201230-82-2 carbon monoxide 
• 619-44-3 methyl 4-iodobenzoate 

Relevant articles and documents

An easily accessible resin-supported palladium catalyst for Sonogashira coupling

Readily available aminomethyl-polystyrene beads can be transformed in a one-pot reaction to an air-stable polymer-bound chelate phosphine, which can be used for the immobilization of homogeneous catalysts. Such prepared Pd catalysts have proven to be useful reagents for mediating Sonogashira-coupling reactions.

Photoredox-Catalyzed Stereoselective Conversion of Alkynes into Tetrasubstituted Trifluoromethylated Alkenes

A regio- and stereoselective synthesis of trifluoromethylated alkenes bearing four different substituents has been developed. Stereocontrolled sulfonyloxytrifluoromethylation of unsymmetric internal alkynes with an electrophilic CF3 reagent, namely the triflate salt of the Yagupol'skii-Umemoto reagent, in the presence of an Ir photoredox catalyst under visible-light irradiation afforded trifluoromethylalkenyl triflates with well-predictable stereochemistry resulting from anti addition of the trifluoromethyl and triflate groups. Subsequent palladium-catalyzed cross-couplings led to tetrasubstituted trifluoromethylated alkenes in a highly stereoselective manner. The present method is the first example of a facile one-pot synthesis of tetrasubstituted trifluoromethylated alkenes from simple alkynes.

Use of functionalized onium salts as a soluble support for organic synthesis

The invention relates to the use of a onium salt functionalized by at least one organic function, as a soluble support, in the presence of at least one organic solvent, for organic synthesis of a molecule, in a homogenous phase, by at least one transformation of said organic function. The onium salt enables the synthesized molecule to be released. The onium salt is present in liquid or solid form at room temperature and corresponds to formula A1+, X1?, wherein A1+ represents a cation and X1? represents an anion.