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Cinnamyl alcohol has a distinctive odor described as "sweet, balsam, hyacinth, spicy, green, powdery, cinnamic" and is used in perfumery [4] and as a deodorant. Cinnamyl alcohol is the starting material used in the synthesis of reboxetine .
Cinnamyl acetate (3-phenylprop-2-enyl acetate) is a chemical compound of the cinnamyl ester family, in which the variable R group is substituted by a methyl group. As a result of the non-aromatic carbon-carbon double bond, cinnamyl acetate can exist in a Z and an E configuration : [ 9 ]
Cinnamaldehyde is an organic compound with the formula or C₆H₅CH=CHCHO. Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor. [1] It is a phenylpropanoid that is naturally synthesized by the shikimate pathway. [2]
Crotyl groups attached to R. A crotyl group is an organic functional group with the formula RCH 2 CH=CHCH 3. [1] Systematically, it is called a but-2-en-1-yl group and exhibits geometric isomerism, being either cis (Z) or trans (E).
If the alkyl group is not attached at the end of the chain, the bond position to the ester group is suffixed before "-yl": CH 3 CH 2 CH(CH 3)OOCCH 2 CH 3 may be called butan-2-yl propanoate or butan-2-yl propionate. [citation needed]. The prefix form is "oxycarbonyl-" with the (R') group preceding.
The molecular formula C 11 H 12 O 2 (molar mass: ... Cinnamyl acetate; 2,2-Di-2-furylpropane; Ethyl cinnamate This page was last edited on 28 August 2022, at 14: ...
The molecular formula C 9 H 10 O (molar mass: 134.17 g/mol) may refer to: Allyl phenyl ether; Anol; Chavicol; Chromane; Cinnamyl alcohol; 4-Ethylbenzaldehyde; Hydrocinnamaldehyde; Phenylacetone; Propiophenone; 4-Vinylanisole
Methyl cinnamate is the methyl ester of cinnamic acid and is a white or transparent solid with a strong, aromatic odor. It is found naturally in a variety of plants, including in fruits, like strawberry, and some culinary spices, such as Sichuan pepper and some varieties of basil. [4]