36185-09-8

Basic information

• Product Name: Benzenepropanol, a-2-propynyl-
• CAS NO: 36185-09-8
• Molecular Formula: C12H14O
• Molecular Weight: 174.243
• Mol File: 36185-09-8.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Benzenepropanol, a-2-propynyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanol, a-2-propynyl-(36185-09-8)
• EPA Substance Registry System: Benzenepropanol, a-2-propynyl-(36185-09-8)

Safety Data

• Hazardous Substances Data: 36185-09-8(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 53915-69-8 allenyltributylstannane 
• 103934-08-3 (E)-5-Chloro-1-phenyl-6-trimethylsilanyl-hex-5-en-3-ol 
• 624-65-7 2-propynyl chloride 
• 106-96-7 propargyl bromide 
• 33415-30-4 trichloro(propa-1,2-dienyl)silane 
• 16156-58-4 prop-2-yn-1-ol methanesulfonate 
• 1020850-74-1 trifluoromethanesulfonic acid 6-oxo-2-phenethyl-3,6-dihydro-2H-pyran-4-yl ester 
• 75-16-1 methylmagnesium bromide 
• 18295-60-8 propargyl magnesium bromide 
• 40963-57-3 2-Propynylzinc bromide 
• 122-97-4 3-Phenyl-1-propanol 
• 122-78-1 phenylacetaldehyde 
• 107820-22-4 ethyl prop-2-yn-1-yl carbonate 

Downstream Products

• 73536-68-2 7,8-dihydrokavain 
• 1161948-35-1 (2E)-5-hydroxy-3-methoxy-7-phenyl-2-heptenoic acid methyl ester 
• 1214892-52-0 5-phenethyldihydrofuran-3-one 
• 1226762-94-2 1-phenyl-6-(phenylthio)hex-5-en-3-ol 
• 1274698-84-8 C₁₆H₂₂O₂ 
• 1256348-05-6 C₁₅H₁₆O 
• 1256348-13-6 C₂₁H₂₀S 
• 75072-73-0 phenethyl 1,2-propadienyl ketone 

Relevant articles and documents

Tandem Prins/pinacol reaction for the synthesis of oxaspiro[4.5]decan-1-one scaffolds

A novel Lewis acid catalyzed Prins/pinacol cascade process has been developed for the synthesis of 7-substituted-8-oxaspiro[4.5]decan-1-ones in good yields with excellent selectivity. This is the first example of the synthesis of oxaspirocycles from aldehydes and 1-(4-hydroxybut-1-en-2-yl)cyclobutanol through a cascade of Prins/pinacol rearrangement. This method is applicable to a wide range of aldehydes such as aromatic, aliphatic, heteroaromatic, and α,β-unsaturated aldehydes. This journal is the Partner Organisations 2014.

Mechanochemically Induced Dehydrogenation Coupling and [3+2] Cycloaddition of Indolizines with Allenes Using Piezoelectric Materials

A wide range of indolizines with allenes proceeded smoothly under mechanochemically induced conditions via a [3+2] annulation process, affording various substituted pyrrolo[2,1,5-cd]indolizines in good yields. The reaction efficiency was greatly improved

Distal Alkenyl C-H Functionalization via the Palladium/Norbornene Cooperative Catalysis

A distal-selective alkenyl C-H arylation method is reported through a directed palladium/norbornene (Pd/NBE) cooperative catalysis. The key is to use an appropriate combination of the directing group and the NBE cocatalyst. A range of acyclic and cyclic c