4-メトキシけい皮酸エチル

Ethyl methoxycinnamate

HCID 5281783

基本情報

CAS
1929-30-2
標準SMILES
CCOC(=O)/C=C/c1ccc(OC)cc1
InChIKey
DHNGCHLFKUPGPX-RMKNXTFCSA-N
分子式
C12H14O3
平均分子量
206.24 g/mol
単同位体質量
206.09429431

概要

Ethyl 4-methoxycinnamate is a cinnamate ester.

名称と識別子

優先名称
Ethyl methoxycinnamate
IUPAC
ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate
現地名
4-メトキシけい皮酸エチル
英語名
Ethyl 4-methoxycinnamate
分子式
C12H14O3
分子量
206.24

名称と別名

24393-56-4Ethyl methoxycinnamateEthyl trans-p-methoxycinnamateSolaboost SPFUvsob Bethyl (2E)-3-(4-methoxyphenyl)prop-2-enoateEthyl (E)-p-methoxycinnamateEthyl (E)-4-methoxycinnamateEthyl 3-(4-methoxyphenyl)-2-propenoateMethyl-p-coumaric acid, ethyl esterEthyl (E)-3-(4-methoxyphenyl)-2-propenoateSD418S06XD
名称をさらに表示
4-メトキシけい皮酸エチルTRANS‐4‐メトキシけい皮酸エチル4-メトキシけい皮酸エチルエステル4‐メトキシ‐けい皮酸エチルtrans-4-メトキシけい皮酸エチルETHYL P-METHOXYCINNAMATEEthyl trans-4-methoxycinnamate4-METHOXYCINNAMIC ACID ETHYL ESTERETHYL 3-(4-METHOXYPHENYL)ACRYLATE(E)-Ethyl p-methoxycinnamateEPMCRARECHEM AL BI 0241Ethyl 4-MethoxyciamateEthyl 4-methoxycinmate
3-(4-Methoxyphenyl)-2-propenoic acid, ethyl ester2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl esterDTXSID401308962Ethyl (E)-3-(p-methoxyphenyl)-2-propenoateEINECS 217-679-63-(Methoxyphenyl)-2-propenoic acid, ethyl ester(2E)-3-(4-Methoxyphenyl)-2-propenoic acid ethyl esterAI3-05527

データベース識別子

CAS
1929-30-2、24393-56-4
PubChem CID
5281783
DTXSID
DTXSID401308962
ChEMBL
CHEMBL95956
ChEBI
CHEBI:228868
UNII
SD418S06XD
EC Number
106-617-2、217-679-6
Nikkaji
J184.017G、J199.748C

物性

構造計算による物性

XLogP
3
極性表面積
35.5 Ų
水素結合供与体数
0
水素結合受容体数
3
回転可能結合数
5
重原子数
15

実験および物理化学的性質

CosmeticsUv absorber
SpringerMaterials PropertiesChemical structure
Melting Point49 - 50 °C
Physical DescriptionSolid

物理化学的性質

融点
49 °C · 49°C
沸点
187 °C · 187 °C / 15mmHg
比重(密度)
1.08 · 1.080±0.06 g/cm3(Predicted)
貯蔵温度
Sealed in dry,Room Temperature
溶解性
クロロホルム(微量)、メタノール(微量)
外見
Solid

化学的性質

化学的特性White crystalline, soluble in methanol, ethanol, DMSO and other organic solvents, derived from cinnamon.

安全と法規制

GHS分類

GHS Classification · 4 件

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)

The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

危険有害性情報

Regulatory InformationChemical: 2-Propenoic acid, 3-(4-methoxyphenyl)-, ethyl ester
Other Safety InformationEvaluation - Chemicals not considered for in depth evaluation - Not commercially active in Australia
Hazard Classes and CategoriesAcute Tox. 4 (100%)

安全データ

wgk
3
hs_code
29189900
risk_code
36/37/38
化審法
(3)-1706
safety_code
26-36/37/39-24/25
Hazard Classifications
Acute Tox. 4 Oral

化学と産業

薬理情報

Cellular LocationsMembrane

用途と製造

Use ClassificationCosmetics -> Uv absorber
応用分野 · 2 件

使用Ethyl 4-methoxycinnamate is an derivative of 4-methoxycinnamic acid, an antihyperglycemic/hypoglycemic agent that works by stimulating insulin secretion from pancreas and could be developed into a new potential for therapeutic agent used in type 2 diabetic patients.

一般的な説明Ethyl p-methoxycinnamate (EPMC) is a natural product found in K. galanga and C. zedoaria extracts with anti-inflammatory, antiangiogenic, antifungal, larvicidal, and analgesic activities. It inhibits COX-1 and COX-2 in vitro (IC50s = 1.12 and 0.83 μM, respectively) and reduces IL-1 and TNF-α production in vivo. EPMC inhibits granuloma tissue formation and acts as an analgesic, delaying tail flick time, in a dose-dependent manner in rats. It inhibits blood vessel growth in rat aortic explants (IC50 = 91.9 μg/ml). EPMC (<10 μg/ml) also reduces growth of T. rubrum, A. niger, S. cerevisiae, and E. floccosum and is larvicidal (LC50 = 53.64 ppm) against Ae. aegypti.

調製方法 · 1 件

製造方法Ethyl 4-methoxycinnamate synthesis: 4-Methoxycinnamic Acid (0.60 g, 3.36 mmol) was dissolved in 10 mL of dry N,N-dimethylformamide (DMF) in a 25-mL, roundbottomed flask. Cesium carbonate (1.65 g, 5.06 mmol) was added followed by iodoethane (1.0 mL, 12.5 mmol). The flask was capped (rubber septum) and the heterogeneous mixture stirred vigorously at 50 °C for one hour. After this time, HCl (1.0 M, 4.0 mL) was added to quench the reaction. The liquid was decanted from any remaining solid and extracted with 3 : 1 hexanes/ethyl acetate (2 x 10 mL). The organic layer was washed with brine (20 mL), dried with MgSO4, filtered, and solvent removed. The remaining oil solidified on standing to form colorless prisms.Synthesis of ethyl 4-methoxycinnamate

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関連反応

3 件

化合物ノート

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