382051
4-Hydroxy-3-methoxycinnamaldehyde
98%
Sinônimo(s):
Coniferyl aldehyde
Faça loginpara ver os preços organizacionais e de contrato
About This Item
Fórmula linear:
HOC6H3(OCH3)CH=CHCHO
Número CAS:
Peso molecular:
178.18
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
98%
p.e.
175 °C/5 mmHg (lit.)
pf
80-82 °C (lit.)
grupo funcional
aldehyde
cadeia de caracteres SMILES
COc1cc(\C=C\C=O)ccc1O
InChI
1S/C10H10O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-7,12H,1H3/b3-2+
chave InChI
DKZBBWMURDFHNE-NSCUHMNNSA-N
Descrição geral
4-Hydroxy-3-methoxycinnamaldehyde is an isoflavonoid. It has been isolated from the insecticidally active hot dichloromethane extract of heartwood of Gliricidia sepium, seed kernels of Melia azedarach L and barks of Cinnamomum cebuense.
Aplicação
4-Hydroxy-3-methoxycinnamaldehyde is suitable for use in a study to investigate the antioxidant and antiradical activities of ferulates using a β-carotene-linoleate model system and a DPPH radical scavenging assay, respectively.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
Escolha uma das versões mais recentes:
Já possui este produto?
Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
Os clientes também visualizaram
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
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
Isoflavonoids and a pterocarpan from< i> Gliricidia sepium</i>.
Herath HMTB, et al.
Phytochemistry, 47(1), 117-119 (1998)
Antioxidant and antiradical activity of ferulates.
Karamac M, et al.
Czech Journal of Food Sciences, 23(2), 469-475 (2005)
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
Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.
Entre em contato com a assistência técnica