3-Phenylpropionaldehyde, 95%
3-Phenylpropionaldehyde, 95%
3-Phenylpropionaldehyde, 95%
3-Phenylpropionaldehyde, 95%
Thermo Scientific Chemicals

3-Phenylpropionaldehyde, 95%

CAS: 104-53-0 | C9H10O | 134.178 g/mol
Have Questions?
變更視圖buttonViewtableView
Quantity:
50 g
250 g
1000 g
產品號碼 A10367.18
亦稱為 A10367-18
價格 (TWD)
-
申請報價
Quantity:
50 g
Request bulk or custom format
化學識別
CAS104-53-0
IUPAC Name3-phenylpropanal
Molecular FormulaC9H10O
InChI KeyYGCZTXZTJXYWCO-UHFFFAOYSA-N
SMILESO=CCCC1=CC=CC=C1
檢視更多
規格Specification Sheet規格表
Refractive Index1.5210-1.5300 @ 20?C
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥94.0%
Free acid (titration)≤2.0%
檢視更多
3-Phenylpropionaldehyde is used as a flavoring agent. It is also used in the preparation of cinnamaldehyde, 2-chloro hydrocinnamaldehyde by alfa chlorination and mixture of homopropargyl alcohols. It serves as a precursor for the synthesis of mixture of syn- and anti-beta-hydroxyallylsilanes by hydroboration of allenylsilane. It is also involved in the catalytic asymmetric cyanosilylation to prepare (2S)-2-hydroxy-4-phenylbutanenitrile. Further, it undergoes Henry reaction to form nitroaldols by reacting with nitromethane.

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.

Applications
3-Phenylpropionaldehyde is used as a flavoring agent. It is also used in the preparation of cinnamaldehyde, 2-chloro hydrocinnamaldehyde by alfa chlorination and mixture of homopropargyl alcohols. It serves as a precursor for the synthesis of mixture of syn- and anti-beta-hydroxyallylsilanes by hydroboration of allenylsilane. It is also involved in the catalytic asymmetric cyanosilylation to prepare (2S)-2-hydroxy-4-phenylbutanenitrile. Further, it undergoes Henry reaction to form nitroaldols by reacting with nitromethane.

Solubility
Miscible with chloroform, dichloromethane, ethyl acetate, alcohol and ether. Immiscible with water.

Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. Durndell, L. J.; Wilson, K.; Lee, A. F. Platinum-catalysed cinnamaldehyde hydrogenation in continuous flow. RSC Adv. 2015, 5 (97), 80022-80026.
  2. Kashyap, B.; Phukan, P. CuI catalyzed Barbier type allylation of aldehyde in presence of S1,S2-dipyridin-2-yl ferrocene-1,1'-dicarbothioate as ligand. Indian J. Chem. 2015, 54, 662-670.