98689-60-2

Basic information

• Product Name: Benzene, [(3-pentynyloxy)methyl]-
• Synonyms: 3-pentynyloxymethylbenzene;3-pentynyl benzyl ether;Benzene,[(3-pentynyloxy)methyl];5-benzyloxypent-2-yne;1-benzyloxy-3-pentyne
• CAS NO: 98689-60-2
• Molecular Formula: C12H14O
• Molecular Weight: 174.243
• Mol File: 98689-60-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, [(3-pentynyloxy)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(3-pentynyloxy)methyl]-(98689-60-2)
• EPA Substance Registry System: Benzene, [(3-pentynyloxy)methyl]-(98689-60-2)

Safety Data

• Hazardous Substances Data: 98689-60-2(Hazardous Substances Data)

Upstream product

• 57618-47-0 5-benzyloxy-1-pentyne 
• 10229-10-4 pent-3-yn-1-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 98689-66-8 (Z)-pent-3-en-1-yloxymethylbenzene 
• 1174000-75-9 (E)-2-(2-benzyloxyethyl)-1-(4-bromophenyl)but-2-en-1-one 
• 791845-43-7 (Z)-1-(benzyloxy)-4-(4’,4’,5’,5’-tetramethyl-1’,3’,2’-dioxaboralanyl)-pent-3-ene 
• 1372206-43-3 C₁₈H₂₇BO₃ 
• 10229-10-4 pent-3-yn-1-ol 
• 119968-36-4 5-benzyloxy-2-(dimethylphenylsilyl)-2-pentene 
• 119968-35-3 2,3-bis(dimethylphenylsilyl)-5-benzyloxy-2-pentene 
• 98689-65-7 (E)-5-benzyloxy-2-dimethylphenylsilyl-2-pentene 
• 104066-62-8 (E)-5-benzyloxy-3-dimethylphenylsilyl-2-pentene 

Relevant articles and documents

Ligand-Enabled, Copper-Catalyzed Regio- and Stereoselective Synthesis of Trialkylsubstituted Alkenylboronates from Unactivated Internal Alkynes

We report the first copper-catalyzed regio- and stereoselective borylalkylation of dialkylsubstituted internal alkynes with bis(pinacolato)diboron and alkyl halides. A catalytically generated borylcopper species containing a novel π-accepting N-heterocycl

Preparation of iniidazolin-2-iminato molybdenum and tungsten benzylidyne complexes: A new pathway to highly active alkyne metathesis catalysts

The reaction of [PhC=MBr3(dme)] (dme = 1,2-dimethoxyethane) with the hexafluoro-fert-butoxides LiJ. or KX [X = OC(CF3)2Me] afforded the benzylidyne complexes [PhC=MX3(dme)] (2a: M = W, 2b: M = Mo), which further

Highly selective hydrogenation of multiple carbon-carbon bonds promoted by nickel(0) nanoparticles

A new method for the highly stereoselective cis semihydrogenation of internal alkynes, semihydrogenation of terminal alkynes, reduction of dienes to alkenes, and reduction of alkynes and alkenes to alkanes is described based on in situ generated both Ni(0) nanoparticles and molecular hydrogen.