382051
4-羟基-3-甲氧基肉桂醛
98%
别名:
松柏醛
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关于此项目
线性分子式:
HOC6H3(OCH3)CH=CHCHO
化学文摘社编号:
分子量:
178.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-278-4
MDL number:
Assay:
98%
产品名称
4-羟基-3-甲氧基肉桂醛, 98%
InChI key
DKZBBWMURDFHNE-NSCUHMNNSA-N
InChI
1S/C10H10O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-7,12H,1H3/b3-2+
SMILES string
COc1cc(\C=C\C=O)ccc1O
assay
98%
bp
175 °C/5 mmHg (lit.)
mp
80-82 °C (lit.)
functional group
aldehyde
Quality Level
Application
4-羟基-3-甲氧基肉桂醛适用于研究阿魏酸的抗氧化和抗自由基活性-胡萝卜素-亚油酸酯模型系统和 DPPH 自由基清除分析。
General description
4-羟基-3-甲氧基肉桂醛是异黄酮。它从墨西哥丁香心材、苦楝种子仁和肉桂树皮的杀虫活性热二氯甲烷提取物中分离出来。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Antioxidant and antiradical activity of ferulates.
Karamac M, et al.
Czech Journal of Food Sciences, 23(2), 469-475 (2005)
Seikwan Oh et al.
Archives of pharmacal research, 29(6), 469-475 (2006-07-13)
A series of yakuchinone B 1f and its analogs 1a-e was synthesized and evaluated for free radical scavenging, suppression of LPS-induced NO generation, cytotoxicity and anti-excitotoxicity in vitro. Compound 1c exhibited potent anti-excitotoxicity, while all compounds 1a-f showed considerable effects
María C Carpinella et al.
Journal of agricultural and food chemistry, 53(8), 2922-2927 (2005-04-14)
In the continuous search for antifungal compounds from plants, the hydroxycoumarin scopoletin (1) was isolated from seed kernels of Melia azedarach L. from which three other compounds, vanillin (2), 4-hydroxy-3-methoxycinnamaldehyde (3), and (+/-) pinoresinol (4), have also been isolated. Guided
Isoflavonoids and a pterocarpan from< i> Gliricidia sepium</i>.
Herath HMTB, et al.
Phytochemistry, 47(1), 117-119 (1998)
M Lisa Manier et al.
Journal of the American Society for Mass Spectrometry, 22(8), 1409-1419 (2011-09-29)
Isoniazid (INH) is an important component of front-line anti-tuberculosis therapy with good serum pharmacokinetics but unknown ability to penetrate tuberculous lesions. However, endogenous background interferences hinder our ability to directly analyze INH in tissues. Chemical derivatization has been successfully used
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