Hydrocinnamaldehyde

Names
Preferred IUPAC name

3-Phenylpropanal

Other names

3-phenylpropional, 3-phenylpropionaldehyde/ß-Phenylpropionaldehyde

Identifiers

CAS Number

* 104-53-0

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:39940

ChEMBL |

* ChEMBL440161

ChemSpider |

* 7421

EC Number |

* 203-211-8

PubChem CID

* 7707

UNII |

* LP1E86N30T

InChI

* InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H,4,7H2

Key: YGCZTXZTJXYWCO-UHFFFAOYSA-N

SMILES

* C1=CC=C(C=C1)CCC=O

Properties

Chemical formula

| C9H10O
Molar mass | 134.178 g·mol−1
Appearance  | colorless liquid
Density | 1.018 g/cm3
Melting point |  −42 °C (−44 °F; 231 K)
Boiling point |  224 °C (435 °F; 497 K)
Hazards
GHS pictograms |
GHS Signal word | Warning

GHS hazard statements

| H315, H319

GHS precautionary statements

| P264, P280, P302+352, P305+351+338, P321, P332+313, P337+313, P362

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Hydrocinnamaldehyde is the organic compound with the formula C6H5CH2CH2CHO. It is produced by the hydrogenation of cinnamaldehyde. The compound is used in many mechanistic studies.[1] It is a common substrate in organic synthesis.[2][3]

## References

1. ↑ Enache, Dan I.; Edwards, Jennifer K.; Landon, Philip; Solsona-Espriu, Benjamin; Carley, Albert F.; Herzing, Andrew A.; Watanabe, Masashi; Kiely, Christopher J. et al. (2006). "Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Au-Pd/TiO2 Catalysts". Science 311 (5759): 362–365. doi:10.1126/science.1120560. PMID 16424335. Bibcode: 2006Sci...311..362E.
2. ↑ Sasai, Hiroaki; Watanabe, Shizue; Suzuki, Takeyuki; Shibasaki, Masakatsu (2002). "Catalytic Asymmetric Synthesis of Nitroaldols Using a Lanthanum-Lithium-Binol Complex: (2S,3S)-2-Nitro-5-Phenyl-1,3-Pentanediol". Organic Syntheses 78: 14. doi:10.15227/orgsyn.078.0014.
3. ↑ Abbott, Jason; Allais, Christophe; Roush, William R. (2015). "Enantioselective Reductive Syn-Aldol Reactions of 4-Acryloylmorpholine: Preparation of (2R, 3S)-3-Hydroxy-2-methyl-1-morpholino-5-phenylpentan-1-one". Organic Syntheses 92: 38–57. doi:10.15227/orgsyn.092.0038.

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*[CID]: Compound ID
*[H315]: Causes skin irritation
*[H319]: Causes serious eye irritation
*[P264]: Wash … thoroughly after handling
*[P280]: Wear protective gloves/protective clothing/eye protection/face protection
*[P302+352]: IF ON SKIN: Wash with soap and water
*[P305+351+338]: IF IN EYES: Rinse continuously with water for several minutes. Remove contact lenses if present and easy to do – continue rinsing
*[P321]: Specific treatment (see … on this label)
*[P332+313]: If skin irritation occurs: Get medical advice/attention
*[P337+313]: Get medical advice/attention
*[P362]: Take off contaminated clothing and wash before reuse