881851-79-2

Basic information

• Product Name: 1-Naphthalenol, 1,2,3,4-tetrahydro-2-phenyl-, (1S,2R)-
• CAS NO: 881851-79-2
• Molecular Formula: C16H16O
• Molecular Weight: 224.302
• Mol File: 881851-79-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Naphthalenol, 1,2,3,4-tetrahydro-2-phenyl-, (1S,2R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Naphthalenol, 1,2,3,4-tetrahydro-2-phenyl-, (1S,2R)-(881851-79-2)
• EPA Substance Registry System: 1-Naphthalenol, 1,2,3,4-tetrahydro-2-phenyl-, (1S,2R)-(881851-79-2)

Safety Data

• Hazardous Substances Data: 881851-79-2(Hazardous Substances Data)

Upstream product

• 7498-87-5 2-phenyl-3,4-dihydro-2H-naphthalen-1-one 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 20669-52-7 3-phenyl-1,2-dihydronaphthalene 

Relevant articles and documents

Pd-Catalyzed Stereoselective 1,2-Aryboration of Alkenylarenes

The palladium-catalyzed highly regio- and diastereoselective arylboration of alkenylarenes has been developed. This chemistry afforded the benzylic boronic esters with a broad substrate scope, which are valuable synthetic intermediates for organic synthes

Asymmetric transfer hydrogenation of α,β-unsaturated, α-tosyloxy and α-substituted ketones

Asymmetric transfer hydrogenation of cyclic and acyclic α,β-unsaturated ketones catalysed by η6-p-cymene/ ruthenium(II) and η5-pentamethylcyclopentadienyl/rhodium(III) complexes have been investigated. Cyclic α,β-unsaturated ketones appeared to be more suitable substrates for the synthesis of enantiomerically pure allylic alcohols than do acyclic α,β-unsaturated ketones. A proposed mechanism for the formation of 4-phenyl-[1,3]-dioxolan-2-one from α-tosyloxy- and halo-substituted acetophenones is discussed. The results of further investigations into the reduction of a range of α- tosyloxyacetophenones and the dynamic kinetic resolution of α-substituted ketones is presented.