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1-Phenyl-1-propyne / 5 G

Purity: 99 %
Synonym: Prop-1-ynylbenzene; Prop-1-yn-1-ylbenzene; C9H8
Molecular Formula: C6H5C‰¡CCH3
Molecular Weight: 116.16
SKU: MND-51092
CAS Number: 673-32-5
MDL number: MFCD00009272
EC Number: 211-607-7
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 G  
66.29 EUR



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P305 + P351 + P338
P261
P271
P302 + P352

Pictograms



Properties

Signal WordWarning
Flash Point (C)62 °C - closed cup
Flash Point (F)143.6 °F - closed cup
Density0.928 g/mL at 25 °C (lit.)
Boiling Point185 °C (lit.)

 Product Description

1-Phenyl-1-propyne is an organic compound with a phenyl group attached to a propyne moiety. It is commonly used as a reagent in organic synthesis, particularly in the preparation of substituted alkynes and aromatic compounds.

 

Application:

1-Phenyl-1-propyne serves as a versatile building block in organic chemistry, utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It undergoes various transformations such as Sonogashira coupling and hydroamination reactions to introduce functional groups into organic molecules.

 

 

Articles:

- A comparative study of Pd supported on MCM-41 and SiO2 in the liquid phase hydrogenation of phenyl alkyl acetylenes mixtures

Publication Date: Available online 27 January 2005

N. Marín-Astorga, G. Pecchi, J.L.G. Fierro, P. Reyes

https://doi.org/10.1016/j.molcata.2005.01.004

 

- Nitrogen permeability and carbon dioxide solubility in poly(1-trimethylsilyl-1-propyne)-based binary substituted polyacetylene blends

Publication Date: Available online 15 December 2004

Kazukiyo Nagai, Shinji Kanehashi, Shingo Tabei, Tsutomu Nakagawa

https://doi.org/10.1016/j.memsci.2004.10.041

 

- Chain transfer reaction to terminal olefins in the polymerization of 1-phenyl-1-propyne with Nb and Ta catalysts

Publication Date: November 1993

Hiroaki Kouzai, Toshio Masuda, Toshinobu Higashimura

https://doi.org/10.1002/macp.1993.021941122