3-Fenil-1-propino, 97 %, estabilizado, Thermo Scientific Chemicals
3-Fenil-1-propino, 97 %, estabilizado, Thermo Scientific Chemicals
3-Fenil-1-propino, 97 %, estabilizado, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Fenil-1-propino, 97 %, estabilizado, Thermo Scientific Chemicals

CAS: 10147-11-2 | C9H8 | 116.163 g/mol
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Número de catálogoCantidad
H53500.14
también denominado H53500-14
25 g
Número de catálogo H53500.14
también denominado H53500-14
Precio (USD)
-
Cantidad:
25 g
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Identificadores químicos
CAS10147-11-2
IUPAC Name(prop-2-yn-1-yl)benzene
Molecular FormulaC9H8
InChI KeyNGKSKVYWPINGLI-UHFFFAOYSA-N
SMILESC#CCC1=CC=CC=C1
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EspecificacionesSpecification SheetHoja de especificaciones
Infrared 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.

Aplicaciones
El 3-fenil-1-propino se utiliza como material de partida en la síntesis del 4-fenil-2-butin-1-ol. También se utiliza en la preparación de beta-hidroxitriazoles e indoles.

Notas
Incompatible con ácidos y bases.
RUO – Research Use Only

General References:

  1. 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.
  2. 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.