36229-72-8

Basic information

• Product Name: 2,3-Bis-(1-hydroxy-3-phenylprop-2-inyl)-naphthalin
• Synonyms: 2,3-Bis-(1-hydroxy-3-phenylprop-2-inyl)-naphthalin
• CAS NO: 36229-72-8
• Molecular Weight: 388.466
• Mol File: 36229-72-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,3-Bis-(1-hydroxy-3-phenylprop-2-inyl)-naphthalin(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Bis-(1-hydroxy-3-phenylprop-2-inyl)-naphthalin(36229-72-8)
• EPA Substance Registry System: 2,3-Bis-(1-hydroxy-3-phenylprop-2-inyl)-naphthalin(36229-72-8)

Safety Data

• Hazardous Substances Data: 36229-72-8(Hazardous Substances Data)

Upstream product

• 42189-19-5 2,3-dibenzoylanthracene 
• 536-74-3 phenylacetylene 
• 7149-49-7 2,3-naphthalenedicarboxaldehyde 

Downstream Products

• 31272-88-5 2,3-Bis(1-oxo-phenylpropargyl)naphthalin 
• 26903-74-2 5-Phenyl-pentacen-6,13-chinon 
• 1255101-83-7 5-(4-(trifluoromethyl)phenyl)-14-phenylpentacene 
• 1113009-68-9 acetic acid 1-[3-(1-acetoxy-3-phenyl-prop-2-ynyl)-naphthalen-2-yl]-3-phenyl-prop-2-ynyl ester 

Relevant articles and documents

Isoacenofuran: A novel quinoidal building block for efficient access to high-ordered polyacene derivatives

Herein, a simple and practical method for generating isoacenofuran, a new π-extended quinoidal building block, was developed. A three-step protocol involving double nucleophilic additions of alkynyllithiums to acene-2,3-dicarbaldehyde, mono-oxidation, and acid-promoted cyclization enables the generation of the target molecule, which is trapped by a dienophile to produce highly condensed acenequinones. Further transformations by double nucleophilic additions of alkynyllithium to hexacenequinone, followed by reductive aromatization, produce tetraalkynylhexacenes with a remarkably higher stability than that of the previously reported substituted hexacenes.

Gold-catalyzed cascade cycloisomerization of 1,7-diyn-3,6-bis(propargyl carbonate)s: Stereoselective synthesis of naphtho[b]cyclobutenes

Gold-catalyzed cycloisomerization of 1,7-diyn-3,6-bis(propargyl carbonate)s leads to a highly efficient and diastereoselective synthesis of functionalized naphtho[b]cyclobutenes. A cascade sequence involving gold-catalyzed double 3,3-rearrangement, 6π-electrocyclic reaction and a decarbonylative cyclization was proposed for this reaction.

Highly efficient Bronsted acid-catalyzed cycloisomerizations of alkynes bearing bis(acetoxy) groups to indenyl ketones

A Bronsted acid-catalyzed cycloisomerization of functionalized alkynes is described, which is assumed to be initiated through the formation of a benzylic cation intermediate. The reaction offers a highly efficient and straightforward route to indenyl ketones with a wide range of substituents under mild conditions.