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Phenylpropiolaldehyde
- Name Phenylpropiolaldehyde
- CAS 2579-22-8
- Purity 99%
Product Details
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1.What is the Phenylpropiolaldehyde ?
Phenylpropiolaldehyde is an aromatic aldehyde with the molecular formula C9H6O, featuring a phenyl group and a propynyl group attached to the aldehyde functional group. It is known for its strong and distinctive odor, making it a versatile compound used in various industries.
2.What is the CAS number for Phenylpropiolaldehyde ?
The CAS number of Phenylpropiolaldehyde is 2579-22-8.
3.What are another words for Phenylpropiolaldehyde ?
Synonyms?for?Phenylpropiolaldehyde 2579-22-8:Propiolaldehyde,phenyl- (6CI,7CI,8CI);3-Phenyl-2-propyn-1-al;3-Phenyl-2-propynal;3-Phenylpropynal;Benzenepropiolaldehyde;Formylphenylacetylene;NSC 47568;Phenylacetylenecarboxaldehyde;Phenylpropargylaldehyde;Phenylpropiolaldehyde;Phenylpropynal;3-phenylprop-2-ynal;
4.What is Phenylpropiolaldehyde (2579-22-8) used for?
Used in Pharmaceutical Industry:
Phenylpropiolaldehyde is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and enhance the properties of existing ones.
Used in Fragrance Industry:
It serves as a key component in the creation of fragrances, leveraging its strong and distinctive odor to contribute to the unique scents of perfumes and other scented products.
Used in Chemical Synthesis:
Phenylpropiolaldehyde is utilized as a reagent in organic synthesis, playing a crucial role in the production of a wide range of chemical compounds.
Used in Food Industry:
It is employed as a flavoring agent, adding unique taste and aroma profiles to various food products, enhancing their overall sensory appeal.
However, due to its potential health and environmental risks, Phenylpropiolaldehyde is considered a hazardous substance and should be handled with care to mitigate any associated risks.
InChI:InChI=1/C9H6O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H
Relevant articles related to Phenylpropiolaldehyde:
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P-Stereogenic Phosphines Directed Copper(I)-Catalyzed Enantioselective 1,3-Dipolar Cycloadditions |
Gan, Zhenjie,Zhi, Mengna,Han, Ruiping,Li, Er-Qing,Duan, Zheng,Mathey, Fran?ois , p. 2782 - 2785 (2019) |
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Copper-catalyzed TEMPO addition to propargyl alcohols for the synthesis of vinylic alkoxyamines |
Kang, Ye-Won,Choi, Yoon-Jeong,Jang, Hye-Young , p. 4842 - 4845 (2014) |
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A practical synthesis of phenylpropargyl aldehyde from phenylacetylene and N-formylmorpholine |
Zanka, Atsuhiko , p. 46 - 48 (2000) |
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