134519-88-3

Basic information

• Product Name: 4,4'-(1,4-phenylene)bis(but-3-yn-1-ol)
• Synonyms: 4,4'-(1,4-phenylene)bis(but-3-yn-1-ol)
• CAS NO: 134519-88-3
• Molecular Weight: 214.264
• Mol File: 134519-88-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,4'-(1,4-phenylene)bis(but-3-yn-1-ol)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-(1,4-phenylene)bis(but-3-yn-1-ol)(134519-88-3)
• EPA Substance Registry System: 4,4'-(1,4-phenylene)bis(but-3-yn-1-ol)(134519-88-3)

Safety Data

• Hazardous Substances Data: 134519-88-3(Hazardous Substances Data)

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 927-74-2 3-Butyn-1-ol 
• 624-38-4 para-diiodobenzene 
• 17869-75-9 4-(trimethylsilyloxy)-1-butyne 

Downstream Products

• 1000861-09-5 1,4-bis(4-bromobut-1-yn-1-yl)benzene 
• 134520-19-7 1,4-bis[4-(p-toluenesulfonyloxy)-1-butynyl]benzene 
• 832688-84-3 1,4-bis(4-oxobutyl)benzene 
• 21240-37-9 4-[4-(4-hydroxybutyl)phenyl]butan-1-ol 

Relevant articles and documents

Synthesis of functionalized alkynes via palladium-catalyzed Sonogashira reactions

A highly efficient protocol for the copper and phosphine free Sonogashira cross-coupling reactions of aryl iodides with terminal alkynes under aerobic conditions has been developed. Using 1 mol % of the palladium-bis(oxazoline) complex, Pd-BOX A, in the p

Synthesis of strapped porphyrins: Toward isolation of the chromophore on semiconductor surfaces

Figure presented Strapped porphyrins, designed to bind planar to semiconductor surfaces, were synthesized as model dyes to study the sensitization processes on metal oxide semiconductor nanoparticles surfaces. The strap was added to limit porphyrin-porphy

Synthesis of planar-chiral paracyclophanes via samarium(II)-catalyzed intramolecular pinacol coupling

(Chemical Equation Presented) A series of [n]jparacyclophanediols (n = 8-12) was synthesized by samarium-catalyzed pinacol coupling for their ansa-bridge formation. Enantiomerically pure [n]jparacyclophane esters were derived from the diols in a several steps via chiral resolution (for n = 10) or via crystallization-induced asymmetric transformation (for n = 11) by using amino alcohol auxiliaries and their selective cleavages.