기본 정보
- CAS
1929-30-2- 표준 SMILES
CCOC(=O)/C=C/c1ccc(OC)cc1- InChIKey
DHNGCHLFKUPGPX-RMKNXTFCSA-N- 분자식
- C12H14O3
- 평균 분자량
- 206.24 g/mol
- 단동위원소 질량
- 206.09429431
개요
Ethyl 4-methoxycinnamate is a cinnamate ester.
이름 및 식별자
- 우선 이름
- Ethyl methoxycinnamate
- IUPAC
- ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate
- 영어명
- Ethyl 4-methoxycinnamate
- 분자식
- C12H14O3
- 분자량
- 206.24
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- 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
물성
구조 계산 물성
- XLogP
- 3
- 극성 표면적
- 35.5 Ų
- 수소 결합 공여자 수
- 0
- 수소 결합 수용자 수
- 3
- 회전 가능 결합 수
- 5
- 무거운 원자 수
- 15
- 형식 전하
- 0
- 복잡도
- 215
실험 및 물리화학적 성질
물리화학적 성질
- 녹는점
- 49 °C · 49°C
- 끓는 점
- 187 °C · 187 °C / 15mmHg
- 밀도
- 1.08 · 1.080±0.06 g/cm3(Predicted)
- 저장 조건
- Sealed in dry,Room Temperature
- 용해도
- 클로로포름(약간 용해됨), 메탄올(약간 용해됨)
- 물리적 상태
- Solid
- 색상
- 회백색
- 수용성
- 물에 불용성
- BRN
- 2210033 · 2210033
- 주요 응용
- 음식 및 음료
- InChI
- InChI=1S/C12H14O3/c1-3-15-12(13)9-6-10-4-7-11(14-2)8-5-10/h4-9H,3H2,1-2H3/b9-6+
- InChIKey
- DHNGCHLFKUPGPX-RMKNXTFCSA-N
- SMILES
- C(OCC)(=O)/C=C/C1=CC=C(OC)C=C1
- LogP
- 2.65 · 2.650 (est)
- NIST
- Ethyl p-methoxycinnamate(24393-56-4)
화학적 성질
White crystalline, soluble in methanol, ethanol, DMSO and other organic solvents, derived from cinnamon.
안전 및 규제
GHS 분류
GHS Classification
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.
유해성 정보
안전 데이터
- wgk
- 3
- HS 번호
- 29189900
- risk_code
- 36/37/38
- safety_code
- 26-36/37/39-24/25
- Hazard Classifications
- Acute Tox. 4 Oral
- 스토리지 클래스
- 11 - Combustible Solids
화학 및 산업
약리 정보
용도 및 제조
응용 분야
용도Ethyl 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.
일반 설명Ethyl 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.
제조 방법
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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