coniferyl aldehyde
Suppliers
Names
[ CAS No. ]:
458-36-6
[ Name ]:
coniferyl aldehyde
[Synonym ]:
Ferulaldehyde
(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal
(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal
Ferulyl aldehyde
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl), (E)-
4-hydroxy-3-methoxy-benzaldehyde
MFCD00075811
4-hydroxy-3-methoxy-cinnamon-aldehyde
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)-, (2E)-
coniferaldehyde
4-hydroxy-3-methoxycinnamic aldehyde
EINECS 207-278-4
4-HYDROXY-3-METHOXYCINNAMALDEHYDE
(2E)-3-(4-Hydroxy-3-methoxyphenyl)acrylaldehyde
coniferyl aldehyde
Coniferylaldehyde
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
338.8±27.0 °C at 760 mmHg
[ Melting Point ]:
80-82ºC(lit.)
[ Molecular Formula ]:
C10H10O3
[ Molecular Weight ]:
178.185
[ Flash Point ]:
136.8±17.2 °C
[ Exact Mass ]:
178.062988
[ PSA ]:
46.53000
[ LogP ]:
1.35
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.593
[ Storage condition ]:
2-8°C
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
36/37/38
[ Safety Phrases ]:
26-37/39
[ RIDADR ]:
NONH for all modes of transport
[ HS Code ]:
2912499000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2912499000
[ Summary ]:
2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%
Articles
J. Mass Spectrom. 49(8) , 665-73, (2014)
Imaging mass spectrometry (IMS) studies increasingly focus on endogenous small molecular weight metabolites and consequently bring special analytical challenges. Since analytical tissue blanks do not ...
J. Am. Soc. Mass Spectrom. 22(8) , 1409-19, (2011)
Isoniazid (INH) is an important component of front-line anti-tuberculosis therapy with good serum pharmacokinetics but unknown ability to penetrate tuberculous lesions. However, endogenous background ...
J. Agric. Food Chem. 53(8) , 2922-7, (2005)
In the continuous search for antifungal compounds from plants, the hydroxycoumarin scopoletin (1) was isolated from seed kernels of Melia azedarach L. from which three other compounds, vanillin (2), 4...