| Identification | More | [Name]
2'-Methoxycinnamaldehyde | [CAS]
1504-74-1 | [Synonyms]
2-METHOXYCINNAMALDEHYDE
2-PROPENYL-3(2-METHOXYPHENOL)
AKOS BBS-00003213
FEMA 3181
O-METHOXYCINNAMALDEHYDE
O-METHOXY CINNAMIC ALDEHYDE
ORTHO-METHOXY CINNAMIC ALDEHYDE
(2E)-3-(2-Methoxyphenyl)-2-propenal
2-methoxycimnamaldehyde
2-Methoxycinnamic aldehyde
2-propenal,3-(2-methoxyphenyl)-
3-(2-methoxyphenyl)-2-propena
3-(2-methoxyphenyl)-2-Propenal
beta-(o-Methoxyphenyl)acrolein
Cinnamaldehyde, o-methoxy-
o-methoxy-cinnamaldehyd
0-Methoxy Cinnamaldehyde
O-METHOXYCINNAMALDEHYDE 96+%
ORTHO-METHOXYCINNAMALDEHYDE
2′-Methoxycinnamaldehyd | [EINECS(EC#)]
216-131-3 | [Molecular Formula]
C10H10O2 | [MDL Number]
MFCD00007001 | [Molecular Weight]
162.19 | [MOL File]
1504-74-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
2
| [RTECS ]
GD6590000
| [HS Code ]
29124990 |
| Hazard Information | Back Directory | [General Description]
Yellow crystals. | [Reactivity Profile]
Aldehydes, such as O-METHOXYCINNAMALDEHYDE(1504-74-1), are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation. | [Air & Water Reactions]
Insoluble in water. | [Fire Hazard]
This compound is flammable. | [Description]
o-Methoxycinnamaldehyde has a sweet, warm, spicy-floral odor
with fruity undertones. It has a sweet, spicy, warm flavor, somewhat pungent above 200 - 300 ppm. It is formed after a long
contact period between salicylaldehyde and acetaldehyde in
diluted alkaline solution; it can be formed by condensation of
salicylaldehyde methylether with acetaldehyde under alkaline conditions; from the corresponding oxime.
| [Chemical Properties]
o-Methoxycinnamaldehyde has a sweet, warm, spicy-floral odor with fruity undernotes. It has a sweet, spicy, warm
flavor and is somewhat pungent above 200 to 300?ppm. | [Occurrence]
Reported found in cinnamon oil (Cinnamomum cassia Nees ex Bl.) from which it is separated as stearoptene;
in cinnamon bark and leaf. | [Definition]
ChEBI: Cassiastearoptene is a member of cinnamaldehydes. | [Preparation]
It is formed after a long contact period between salicylaldehyde and acetaldehyde in diluted alkaline solution; it may
also be formed by condensation of salicylaldehyde methylether with acetaldehyde under alkaline conditions; from the corresponding
oxime. It may be isolated and purified from powdered cinnamon. | [Taste threshold values]
Taste characteristics at 50 ppm: warm, spicy, cinnamon and clove-like. | [target]
P450 (e.g. CYP17) |
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