(E)-4-メトキシけい皮酸

4-Methoxycinnamic Acid

HCID 699414

基本情報

CAS
830-09-1
標準SMILES
COc1ccc(/C=C/C(=O)O)cc1
InChIKey
AFDXODALSZRGIH-QPJJXVBHSA-N
分子式
C10H10O3
平均分子量
178.18 g/mol
単同位体質量
178.06299418

概要

4-methoxycinnamic acid is a methoxycinnamic acid having a single methoxy substituent at the 4-position on the phenyl ring. It is functionally related to a cinnamic acid.

名称と識別子

優先名称
4-Methoxycinnamic Acid
IUPAC
(E)-3-(4-methoxyphenyl)prop-2-enoic acid
現地名
(E)-4-メトキシけい皮酸
英語名
trans-O-Methyl-p-coumaric acid
分子式
C10H10O3
分子量
178.18

名称と別名

4-Methoxycinnamic acid830-09-13-(4-methoxyphenyl)acrylic acid(E)-3-(4-methoxyphenyl)prop-2-enoic acid(2E)-3-(4-methoxyphenyl)prop-2-enoic acid2-Propenoic acid, 3-(4-methoxyphenyl)-3-(4-Methoxyphenyl)-2-propenoic acidNSC-5303NSC-6234376G4ML8401A3-(4-methoxyphenyl)prop-2-enoic acidCHEBI:48541
名称をさらに表示
(E)-3-(4-メトキシフェニル)アクリル酸(E)-3-(4-メトキシフェニル)プロペン酸(E)-4-メトキシベンゼンプロペン酸4-メトキシけい皮酸(E)-4-メトキシけい皮酸p-メトキシ-trans-けい皮酸4-メトキシ-trans-けい皮酸p-メトキシけい皮酸trans-4-メトキシけい皮酸(E)-3-(4-メトキシフェニル)-2-プロペン酸4-メトキシけい皮酸, 〜98%trans-4-メトキシけい皮酸, 98%(E)-4-Methoxycinnamic acidPMCAAKOS B000181AKOS BB/0034AKOS BBS-00000769TIMTEC-BB SBB005717RARECHEM BK HC T2574-methoxycinmic acidOTAVA-BB BB0123400502
DTXSID4048147RefChem:25958DTXCID4028121212-594-0943-89-5(E)-3-(4-Methoxyphenyl)acrylic acidP-METHOXYCINNAMIC ACIDtrans-4-Methoxycinnamic acid

データベース識別子

CAS
830-09-1、943-89-5
PubChem CID
699414
DTXSID
DTXSID1046059
ChEMBL
CHEMBL95770
ChEBI
CHEBI:48541
UNII
6G4ML8401A
EC Number
212-594-0、213-405-4
Nikkaji
J47.704D、J60.989G

物性

構造計算による物性

XLogP
1.8
極性表面積
46.5 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
3
重原子数
13

実験および物理化学的性質

Chemical ClassesUV filter
SpringerMaterials PropertiesChemical diffusion
LogP · 2 件

2.68

2.68

Solubility0.712 mg/mL at 25 °C
Melting Point173 - 175 °C
Physical DescriptionSolid

物理化学的性質

融点
173.5 °C · 173.5 °C(lit.)
沸点
342.6 · 342.6±17.0 °C(Predicted)
比重(密度)
1.195 · 1.195±0.06 g/cm3(Predicted)
貯蔵温度
Keep in dark place,Sealed in dry,Room Temperature
溶解性
エタノール、酢酸エチル等の有機溶剤に可溶。
酸解離定数(Pka)
4.6 · 4.60±0.10(Predicted)

安全と法規制

GHS分類

GHS Classification · 6 件

Warning

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 54 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Warning

H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]

危険有害性情報

Regulatory Information · 4 件

Chemical: 2-Propenoic acid, 3-(4-methoxyphenyl)-

Chemical: 2-Propenoic acid, 3-(4-methoxyphenyl)-, (E)-

Status: Active Update: 26-04-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/22331

2-Propenoic acid, 3-(4-methoxyphenyl)-, (2E)-: Does not have an individual approval but may be used under an appropriate group standard

Hazard Classes and Categories · 2 件

Skin Irrit. 2 (100%)

Skin Irrit. 2 (100%)

安全データ

F
8
wgk
3
tsca
TSCA listed
rtecs
UD3391300
hs_code
2918.29.7500
risk_code
36/37/38

化学と産業

薬理情報

Cellular LocationsMembrane

用途と製造

General Manufacturing Information · 2 件

2-Propenoic acid, 3-(4-methoxyphenyl)-: ACTIVE

2-Propenoic acid, 3-(4-methoxyphenyl)-, (2E)-: INACTIVE

応用分野 · 1 件

使用Esters derived from trans-4-methoxycinnamic acid are effective absorbers of UV radiation. The starting material was trans-4-methoxycinnamic acid and 3,5dimethoxybenzoic acid methyl ester in isolated avenanthramide alkaloids synthsis. trans-4-Methoxycinnamic acid was converted into its acid chloride (yield 98%) with thionyl chloride. Employed in organic synthesis of pharmaceutical intermediates, synthetic anti-adrenergic drugs esmolol, cosmetics ultraviolet absorption.

調製方法 · 2 件

製造方法4-methoxycinnamic acid synthesis : In a 25-mL, roundbottomed flask, 4-methoxybenzaldehyde (0.804 mL, 6.61 mmol) (3), malonic acid (1.75 g, 16.8 mmol), and β-alanine (0.10 g, 1.12 mmol) were dissolved in pyridine (3.0 mL, 37.1 mmol) and heated under reflux for 90 minutes. After cooling to room temperature, the reaction mixture was placed in an ice bath and 8.0 mL of concentrated HCl was slowly added. The resulting white precipitate was collected by vacuum filtration, washed with cold water (2 x 10mL) and dried thoroughly. The product was recrystallized from absolute ethanol (~20 mL).Synthesis of 4-methoxycinnamic acid

純化方法Crystallise the acid from MeOH to constant melting point and UV spectrum. [Beilstein 10 IV 1005.]

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関連反応

11 件

化合物ノート

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