3-(4-hydroxyphenyl)acrylaldehyde
- Product Name
- 3-(4-hydroxyphenyl)acrylaldehyde
- CAS No.
- 2538-87-6
- Chemical Name
- 3-(4-hydroxyphenyl)acrylaldehyde
- Synonyms
- AT-51103;p-CouMaryl aldehyde;p-Coumaroyl aldehyde;2-Propenal, 3-(4-hydroxyphenyl)-;3-(4-hydroxyphenyl)acrylaldehyde
- CBNumber
- CB32551972
- Molecular Formula
- C9H8O2
- Formula Weight
- 148.16
- MOL File
- 2538-87-6.mol
3-(4-hydroxyphenyl)acrylaldehyde Property
- Melting point:
- 140℃
- Boiling point:
- 309.4±17.0 °C(Predicted)
- Density
- 1.174±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 9.59±0.26(Predicted)
- color
- Pale Yellow to Very Dark Brown
- Stability:
- Light Sensitive
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- C755450
- Product name
- p-Coumaraldehyde
- Packaging
- 1g
- Price
- $620
- Updated
- 2021/12/16
- Product number
- CD12091253
- Product name
- 3-(4-Hydroxyphenyl)acrylaldehyde
- Purity
- 95+%
- Packaging
- 5g
- Price
- $1089
- Updated
- 2021/12/16
- Product number
- 2538876
- Product name
- 3-(4-Hydroxyphenyl)acrylaldehyde
- Packaging
- 5g
- Price
- $1210.99
- Updated
- 2021/12/16
- Product number
- 2538876
- Product name
- 3-(4-Hydroxyphenyl)acrylaldehyde
- Packaging
- 10g
- Price
- $1650.33
- Updated
- 2021/12/16
- Product number
- CD12091253
- Product name
- 3-(4-Hydroxyphenyl)acrylaldehyde
- Purity
- 95+%
- Packaging
- 10g
- Price
- $1683
- Updated
- 2021/12/16
3-(4-hydroxyphenyl)acrylaldehyde Chemical Properties,Usage,Production
Uses
p-Coumaraldehyde is a potential antitumor agents extracted from cucumbers. p-Coumaraldehyde was shown to significantly inhibit the cancer cell growth in a dose-dependent manner
Definition
ChEBI: A cinnamaldehyde that is (E)-cinnamaldehyde substituted at position 4 on the phenyl ring by a hydroxy group.
Synthesis
103909-81-5
2538-87-6
General method: compounds 8a2, 8b2 and 8d2 were dissolved in methanol and a catalytic amount of p-toluenesulfonic acid (p-TsOH) was added. After stirring the reaction mixture for 1 h at room temperature, the solvent was evaporated under reduced pressure. Water was added to the residue and extracted with ethyl acetate (EtOAc). The organic layers were combined and dried over anhydrous sodium sulfate (Na2SO4) and subsequently concentrated under reduced pressure. The resulting residue was purified by column chromatography to afford analogs 8a1, 8b1 and 8d1 of the target product 3-(4-hydroxyphenyl)acrolein.
References
[1] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 13, p. 2839 - 2844
3-(4-hydroxyphenyl)acrylaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
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