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112372

Sigma-Aldrich

Ethyl cinnamate

99%

Sinónimos:

3-Phenyl-2-propenoic acid ethyl ester, Ethyl 3-phenyl-2-propenoate, NSC 6773

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About This Item

Fórmula lineal:
C6H5CH=CHCOOC2H5
Número de CAS:
103-36-6
Peso molecular:
176.21
Beilstein:
775541
Número CE:
203-104-6
Número MDL:
MFCD00009189
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
24847091
NACRES:
NA.22

Nivel de calidad

100

Ensayo

99%

impurezas

may contain alpha-tocopherol (synthetic)

índice de refracción

n20/D 1.558 (lit.)

bp

271 °C (lit.)

mp

6-8 °C (lit.)

densidad

1.049 g/mL at 20 °C (lit.)

temp. de almacenamiento

2-8°C

cadena SMILES

CCOC(=O)\C=C\c1ccccc1

InChI

1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+

Clave InChI

KBEBGUQPQBELIU-CMDGGOBGSA-N

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Aplicación

  • Antimicrobial and antiproliferative effects: Essential oils including Ethyl cinnamate derived from Zingiberaceae family show promising antimicrobial and antiproliferative properties, suggesting their potential application in oral healthcare products. This study provides insight into the utilization of natural products for medical and pharmaceutical applications (Amil et al., 2024).
  • Biodistribution and cellular interactions in medical research: Ethyl cinnamate could be investigated for its role in enhancing the permeability and imaging contrast in studies like those investigating the biodistribution of intravenously delivered mesenchymal stromal cells. Such applications could improve understanding in cellular therapies and regenerative medicine (Pichardo et al., 2022).

Acciones bioquímicas o fisiológicas

Ethyl cinnamate inhibits the growth of Chlorella pyrenoidosa.

Otras notas

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificados de análisis (COA)

Lot/Batch Number
SDBB1621
STBL4204
STBL3440
STBL1830
STBL2297

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Sigma-Aldrich

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Benzyl ether 98%

Sigma-Aldrich

108014

Benzyl ether

ETHYL 2-CHLORO-ALPHA-CYANO-4-(DIMETHYLAMINO)-CINNAMATE AldrichCPR

S529907

ETHYL 2-CHLORO-ALPHA-CYANO-4-(DIMETHYLAMINO)-CINNAMATE

Li-Li Gao et al.
Huan jing ke xue= Huanjing kexue, 34(1), 156-162 (2013-03-16)
The effects of ethyl cinnamate on the growth and physiological characteristics of Chlorella pyrenoidosa were studied. The allelopathic mechanisms were explored, from views of chlorophyll a content, antioxidant enzyme activities, reactive oxygen species (ROS) level, malondialdehyde (MDA) content and photosynthetic
Gessica D Gonçalves et al.
Anatomical record (Hoboken, N.J. : 2007), 303(10), 2668-2678 (2020-01-28)
Fetal hypoxia is a common complication of pregnancy. We have previously reported that maternal hypoxia in late gestation in mice gives rise to male offspring with reduced nephron number, while females have normal nephron number. Male offspring later develop proteinuria
Rozana Othman et al.
Planta medica, 68(7), 655-657 (2002-07-27)
From the rhizomes of Kaempferia galanga, ethyl cinnamate (EC) was isolated and its vasorelaxant effect was examined on the rat aorta. EC inhibited the tonic contractions induced by high K+ and phenylephrine (PE) in a concentration-dependent manner, with respective IC50
Nam-Jin Kim et al.
Pest management science, 64(8), 857-862 (2008-03-08)
This study was aimed at assessing the toxicity of ethyl cinnamate and ethyl p-methoxycinnamate (EMC) identified in Kaempferia galangal L. (Zingiberaceae) rhizome and another 12 known compounds to third-instar larvae from laboratory-reared Culex pipiens pallens Forskal, Aedes aegypti L. and
K Bratt et al.
Journal of chemical ecology, 27(11), 2253-2262 (2002-01-31)
Pine weevils (Hylobius abietis) fed less on bark of lodgepole pine (Pinus contorta) than on bark of Scots pine (P. sylvestris). Two pine weevil antifeedants, ethyl trans-cinnamate and ethyl 2,3-dibromo-3-phenyl-propanoate, were isolated from bark of lodgepole pine. These two compounds
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