1083053-34-2
1083053-34-2
Chemical Structure
Cinnamyl acetate-13C2
- CAS No.: 1083053-34-2
- Formula:C913C2H12O2
- Molecular Weight:178.20
InChIKey: WJSDHUCWMSHDCR-MBKSGMOPSA-N
SMILES: [13CH3][13C](OC/C=C/C1=CC=CC=C1)=O
Biological Activity: Cinnamyl acetate-13C2 is the 13C-labeled Cinnamyl acetate (HY-N7125). Cinnamyl acetate is a phenylpropanoid ester fragrance ingredient that serves as a precursor for the synthesis of Chloramphenicol (HY-B0239) and butyrolactone costunolide, and possesses antioxidant activity. Cinnamyl acetate is used in the food, cosmetics, personal care, and pharmaceutical industries[1][2][3].
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Cinnamyl acetate-13C2 | Cinnamyl acetate-13C2 is the 13C-labeled Cinnamyl acetate (HY-N7125). Cinnamyl acetate is a phenylpropanoid ester fragrance ingredient that serves as a precursor for the synthesis of Chloramphenicol (HY-B0239) and butyrolactone costunolide, and possesses antioxidant activity. Cinnamyl acetate is used in the food, cosmetics, personal care, and pharmaceutical industries. | |||||||||||||||||||||
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Cinnamyl acetate (Standard) | 99.58% | Cinnamyl acetate (Standard) is the analytical standard of Cinnamyl acetate (HY-N7125). This product is intended for research and analytical applications. Cinnamyl acetate is a phenylpropanoid ester fragrance ingredient that serves as a precursor for the synthesis of Chloramphenicol (HY-B0239) and butyrolactone costunolide, and possesses antioxidant activity. Cinnamyl acetate is used in the food, cosmetics, personal care, and pharmaceutical industries. | ||||||||||||||||||||
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Cinnamyl acetate | 99.39% | Cinnamyl acetate is a phenylpropanoid ester fragrance ingredient that serves as a precursor for the synthesis of Chloramphenicol (HY-B0239) and butyrolactone costunolide, and possesses antioxidant activity. Cinnamyl acetate is used in the food, cosmetics, personal care, and pharmaceutical industries. | ||||||||||||||||||||
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References
- [1]. Qinghua Liang, et al. Theoretical and experimental studies on the separation of cinnamyl acetate and cinnamaldehyde by adsorption onto a β-cyclodextrin polyurethane polymer. RSC Adv. 2017; 7 (69): 43502–43511.
- [2]. Tomke PD, et al. Ultrasound assisted lipase catalyzed synthesis of cinnamyl acetate via transesterification reaction in a solvent free medium. Ultrasonics sonochemistry. 2015 Nov;27:241-246.
- [3]. Dong H, et al. Whole-Cell Biocatalytic Synthesis of Cinnamyl Acetate with a Novel Esterase from the DNA Library of Acinetobacter hemolyticus. Journal of agricultural and food chemistry. 2017 Mar 15;65(10):2120-2128. [Content Brief]
