110211-26-2

Basic information

• Product Name: Benzene, 4-nonynyl-
• CAS NO: 110211-26-2
• Molecular Formula: C15H20
• Molecular Weight: 200.324
• Mol File: 110211-26-2.mol

Chemical Properties

• CAS DataBase Reference: Benzene, 4-nonynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 4-nonynyl-(110211-26-2)
• EPA Substance Registry System: Benzene, 4-nonynyl-(110211-26-2)

Safety Data

• Hazardous Substances Data: 110211-26-2(Hazardous Substances Data)

Upstream product

• 1220698-71-4 1-phenyl-4-nonyn-3-yl formate 
• 110211-21-7 1-phenylnon-4-yn-3-yl acetate 

Relevant articles and documents

Palladium-Catalyzed Synthesis of Alkynes via a Tandem Decarboxylation/Elimination of (E)-Enol Triflates

A mild catalytic synthesis of alkynes via a tandem Pd-catalyzed decarboxylation/elimination of enol triflates is described. Key attributes of the method include readily available starting materials, broad functional group tolerance, and the ability to access terminal, internal, and halogenated alkynes. The preliminary scope of the reaction is demonstrated on 25 different examples with yields ranging from 63% to 96%.

Selective synthesis of allenes and alkynes through ligand-controlled, palladium-catalyzed decarboxylative hydrogenolysis of propargylic formates

Ligand-controlled regioselective palladium-catalyzed decarboxylative hydrogenolysis of propargylic formates is described. A wide range of allenes and alkynes were obtained by using either 1,2-diphenylphosphinoethane (DPPE) or 1,6-bisdiphenylphosphinohexane (DPPH) as a catalyst ligand.

PALLADIUM-CATALYZED REDUCTION OF PROPARGYLIC ACETATES WITH SmI2. A MILD AND CONVENIENT METHOD FOR THE PREPARATION OF ALLENES

A highly regioselective reduction of propargylic acetates has been attained by using SmI2 and catalytic Pd(0) in the presence of 2,4-dimethyl-3-pentanol affording various types of allenes in high yields.