Ethyl methoxycinnamate

HCID 5281783

Grundinformationen

CAS
1929-30-2
Standard-SMILES
CCOC(=O)/C=C/c1ccc(OC)cc1
InChIKey
DHNGCHLFKUPGPX-RMKNXTFCSA-N
Summenformel
C12H14O3
Durchschnittliche Molmasse
206,24 g/mol
Monoisotopische Masse
206,09429431

Überblick

Ethyl 4-methoxycinnamate is a cinnamate ester.

Namen und Bezeichner

Bevorzugter Name
Ethyl methoxycinnamate
IUPAC
ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate
Englischer Name
Ethyl 4-methoxycinnamate
Summenformel
C12H14O3
Molmasse
206.24

Namen und Synonyme

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
Weitere Namen anzeigen
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

Datenbank-Bezeichner

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

Eigenschaften

Berechnete Struktureigenschaften

XLogP
3
Polarare Oberfläche (TPSA)
35,5 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
3
Frei drehbare Bindungen
5
Schwere Atome
15

Experimentelle und physikochemische Eigenschaften

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

Physikochemische Eigenschaften

Schmelzpunkt
49 °C · 49°C
Siedepunkt
187 °C · 187 °C / 15mmHg
Dichte
1.08 · 1.080±0.06 g/cm3(Predicted)
storage temp.
Sealed in dry,Room Temperature
Löslichkeit
Chloroform (Slightly), Methanol (Slightly)
Aggregatzustand
Solid

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 4 Einträge

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.

Gefahrenhinweise

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%)

Sicherheitsdaten

wgk
3
hs_code
29189900
risk_code
36/37/38
safety_code
26-36/37/39-24/25
Speicherklasse
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Oral

Chemie und Industrie

Pharmakologische Informationen

Cellular LocationsMembrane

Verwendung und Herstellung

Use ClassificationCosmetics -> Uv absorber
Anwendungen · 1 Eintrag

VerwendenEthyl 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.

Darstellung · 1 Eintrag

synthetischeEthyl 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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