Search
Element Search
Structure Search
Thermo Scientific Chemicals
3-Phenyl-1-propyne, 97%, stab.
CAS: 10147-11-2 | C9H8 | 116.163 g/mol
Have Questions?
Change view
Catalog number H53500.14
also known as H53500-14
Price (TWD)
-
Quantity:
25 g
Chemical Identifiers
CAS10147-11-2
IUPAC Name(prop-2-yn-1-yl)benzene
Molecular FormulaC9H8
InChI KeyNGKSKVYWPINGLI-UHFFFAOYSA-N
SMILESC#CCC1=CC=CC=C1
View more
Specifications
Specification Sheet
Specification SheetInfrared spectrumConforms
Assay from Supplier's CofA≥96.0% (CG)
CommentStabilized with 250 ppm BHT
Appearance (Color)Colorless to yellow
FormLiquid
3-Phenyl-1-propyne is used as a starting material in the synthesis of 4-phenyl-2-butyn-1-ol. It is also used in the preparation of beta-hydroxytriazoles and indoles.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-Phenyl-1-propyne is used as a starting material in the synthesis of 4-phenyl-2-butyn-1-ol. It is also used in the preparation of beta-hydroxytriazoles and indoles.
Notes
Incompatible with acids and bases.
3-Phenyl-1-propyne is used as a starting material in the synthesis of 4-phenyl-2-butyn-1-ol. It is also used in the preparation of beta-hydroxytriazoles and indoles.
Notes
Incompatible with acids and bases.
RUO – Research Use Only
General References:
- Yosihda, H.; Shinke, A.; Kawano, Y.; Takaki, K. Copper-catalyzed α-selective hydrostannylation of alkynes for the synthesis of branched alkenylstannanes. Chem. Commun. 2015, 51 (53), 10616-10619.
- Parker, D. S. N.; Kaiser, R. I.; Kostko, O.; Ahmed, M. Selective Formation of Indene through the Reaction of Benzyl Radicals with Acetylene. ChemPhysChem 2015, 16 (10), 2091-2093.