Interesting facts
Interesting Facts About 3-Phenylpropanal
3-Phenylpropanal is a fascinating compound that belongs to the class of aldehydes. It is often noted for its intriguing molecular structure and distinctive properties. Here are some engaging insights about this compound:
- Structure and Isomerism: The unique structure of 3-phenylpropanal includes a phenyl group attached to a longer carbon chain. This compound is an example of structural isomerism, where the position of the functional group (the aldehyde) can significantly influence the chemical reactivity and physical properties of the compound.
- Natural Occurrence: Aldehydes like 3-phenylpropanal can be found naturally in various essential oils. They're often used in the food industry for flavoring and are known for their aromatic qualities.
- Applications in Synthesis: This compound plays a crucial role in organic synthesis. It is often utilized in the production of more complex organic molecules, making it valuable in pharmaceuticals and agrochemicals.
- Flavor and Fragrance Industry: Owing to its pleasant aroma, 3-phenylpropanal is used in perfumery and is recognized for imparting floral notes in fragrances. It is also explored for potential use in flavoring food products.
- Reactivity: As an aldehyde, 3-phenylpropanal participates in various chemical reactions. Its ability to undergo oxidation reactions makes it interesting for studies related to organic transformations and reaction mechanisms.
As a chemical scientist, understanding compounds like 3-phenylpropanal not only enhances our knowledge of organic chemistry but also opens the doors to innovative applications in various industries. “Chemistry is the art of transformation,” and compounds such as this one exemplify just that.
Synonyms
3-Phenylpropanal
104-53-0
3-Phenylpropionaldehyde
Benzenepropanal
HYDROCINNAMALDEHYDE
Hydrocinnamic aldehyde
Benzylacetaldehyde
Dihydrocinnamaldehyde
3-Phenyl-1-propanal
3-Phenylpropylaldehyde
Phenylpropyl aldehyde
Propanal, phenyl-
Hydrocinnamylaldehyde
3-Phenylpropyl aldehyde
beta-Phenylpropionaldehyde
Propionaidehyde, 3-phenyl-
3-Phenyl-propionaldehyde
Phenylpropionaldehyde
3-Phenylpropan-1-al
FEMA No. 2887
.beta.-Phenylpropionaldehyde
NSC 9271
EINECS 203-211-8
BRN 1071910
LP1E86N30T
1335-10-0
DTXSID0047610
AI3-01377
NSC-9271
EINECS 215-620-9
DTXCID8027610
CHEBI:39940
4-07-00-00692 (Beilstein Handbook Reference)
3-PHENYLPROPIONALDEHYDE [FCC]
3-PHENYLPROPIONALDEHYDE [FHFI]
3PL
3-phenyl propionaldehyde
MFCD00007021
UNII-LP1E86N30T
3phenylpropanal
Phenyl-Propanal
3Phenyl1propanal
hydrocinnamaidehyde
3-phenyl propanal
phenylpropylaldehyde
3Phenylpropylaldehyde
3-phenylproionaldehyde
Benzenepropanal, 9CI
3Phenylpropyl aldehyde
betaPhenylpropionaldehyde
Propionaldehyde, 3phenyl
3-Phenyl-Propionaidehyde
FLUNARIZINE_met002
beta -phenylpropionaldehyde
WLN: VH1UU1R
WLN: VH2R
SCHEMBL1335
UPCMLD00WV-107
CHEMBL440161
FEMA 2887
NSC9271
Tox21_302494
AKOS000120255
AB00823
CS-W007446
FP26997
Hydrocinnamaldehyde, >=95%, FG, FCC
NCGC00256683-01
BP-11455
CAS-104-53-0
DS-13816
Hydrocinnamaldehyde, technical grade, 90%
NS00006643
P0217
3-Phenylpropionaldehyde Hydrocinnamic aldehyde
3-phenylpropionaldehyde;hydrocinnamic aldehyde
EN300-18678
Hydrocinnamaldehyde, analytical reference material
Q174903
Z87002472
F2190-0593
203-211-8
Solubility of 3-phenylpropanal
3-phenylpropanal, a captivating compound in organic chemistry, exhibits interesting solubility characteristics. Being an aldehyde with a phenyl group, its solubility is influenced by both its non-polar and polar properties. Here are some key points to consider:
In summary, "like dissolves like," making polar solvents ideal for 3-phenylpropanal, while its solubility in water is constrained due to its larger hydrophobic phenyl ring. This unique solubility profile contributes to its versatility in synthetic applications and serves as a focal point in understanding the behavior of aldehyde compounds in various environments.