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Benzil sinamat

Benzil sinamat
Skeletal formula of benzyl cinnamate
Space-filling model of the benzyl cinnamate molecule
Nama
Nama IUPAC (preferensi)
Benzil (2E)-3-fenilprop-2-enoat
Nama lain
Benzil sinamat
Sinamein
Benzil sinamoat
Benzil 3-fenilpropenoat
Asam 3-Fenil-2-propenoat ester fenilmetil
Asam sinamat ester benzil
Penanda
Model 3D (JSmol)
ChemSpider
Nomor EC
Nomor RTECS {{{value}}}
UNII
  • InChI=1S/C16H14O2/c17-16(12-11-14-7-3-1-4-8-14)18-13-15-9-5-2-6-10-15/h1-12H,13H2/b12-11+
    Key: NGHOLYJTSCBCGC-VAWYXSNFSA-N
  • C1=CC=C(C=C1)COC(=O)C=CC2=CC=CC=C2
Sifat
C16H14O2
Massa molar 238,29 g·mol−1
Penampilan Padatan putih hingga kuning pucat[1]
Titik lebur 34–37 °C (93–99 °F; 307–310 K)[2]
Titik didih 195–200 °C (383–392 °F; 468–473 K) 5 mmHg[2]
Tidak larut[1]
Kelarutan dalam etanol 125 g/L
Kelarutan dalam gliserin Tidak larut
Kelarutan dalam propilen glikol Tidak larut
Kecuali dinyatakan lain, data di atas berlaku pada suhu dan tekanan standar (25 °C [77 °F], 100 kPa).
Referensi

Benzil sinamat adalah senyawa kimia yang merupakan ester yang berasal dari asam sinamat dan benzil alkohol.

Ketersediaan di alam

Balsam merupakan penghasil utama benzil sinamat.[3]

Kegunaan

Senyawa ini digunakan sebagai:

Referensi

  1. ^ a b "Specifications for Flavourings". Food and Agriculture Organization. Diarsipkan dari asli tanggal 2015-09-24. Diakses tanggal 2014-02-20.
  2. ^ a b "Benzyl cinnamate". Sigma-Aldrich.
  3. ^ a b George A. Burdock (2010), "BENZYL CINNAMATE", Fenaroli's Handbook of Flavor Ingredients (Edisi 6th), CRC Press, hlm. 147–148
  4. ^ Korošec, B.; Sova, M.; Turk, S.; Kraševec, N.; Novak, M.; Lah, L.; Stojan, J.; Podobnik, B.; Berne, S.; Zupanec, N.; Bunc, M.; Gobec, S.; Komel, R. (2014). "Antifungal activity of cinnamic acid derivatives involves inhibition of benzoate 4-hydroxylase (CYP53)". Journal of Applied Microbiology (dalam bahasa Inggris). 116 (4): 955–966. doi:10.1111/jam.12417. ISSN 1365-2672. PMID 24314266.
  5. ^ "Sudocrem Antiseptic Healing Cream - Summary of Product Characteristics (SmPC) - (emc)". www.medicines.org.uk. Diakses tanggal 11 June 2021.

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