160695
2-羟基-4-甲氧基苯甲醛
98%
别名:
4-甲氧基水杨醛
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关于此项目
线性分子式:
HOC6H3(OCH3)CHO
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-604-0
Beilstein/REAXYS Number:
1072443
MDL number:
Assay:
98%
InChI key
WZUODJNEIXSNEU-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-7-3-2-6(5-9)8(10)4-7/h2-5,10H,1H3
SMILES string
[H]C(=O)c1ccc(OC)cc1O
assay
98%
mp
41-43 °C (lit.)
functional group
aldehyde
Quality Level
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General description
2-羟基-4-甲氧基苯甲醛是杠柳根皮精油的主要成分。 它是一种存在于非洲药用植物中的潜在酪氨酸酶抑制剂。
Application
2-二噻烷-4-二醇被用于希夫碱配体的合成。
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
Belagihalli M Srikanta et al.
Biochimie, 93(4), 678-688 (2010-12-28)
Helicobacter pylori mediated gastric ulcer and cancers are common global problems since it was found to colonize in ∼50% of gastric ulcer/cancer patients. Decalepis hamiltonii, (Asclepiadaceae family) extracts have been depicted with medicinal properties supporting the traditional knowledge of health
I Kubo et al.
Planta medica, 65(1), 19-22 (1999-03-20)
By bioassay-guided fractionation using mushroom tyrosinase (EC 1.14.18.1), 2-hydroxy-4-methoxybenzaldehyde was characterized as the principal tyrosinase inhibitor from three East African medicinal plants, the root of Mondia whitei (Hook) Skeels (Asclepiaceae), the root of Rhus vulgaris Meikle (Anacardiaceae), and the bark
Subban Nagarajan et al.
Journal of AOAC International, 86(3), 564-567 (2003-07-11)
The roots of Decalepis hamiltonii and Hemidesmus indicus are aromatic and possess the crystalline compound 2-hydroxy-4-methoxybenzaldehyde as the major compound (> 90%) in their volatile oils. A gas chromatographic procedure was developed for the assay of 2-hydroxy-4-methoxybenzaldehyde in both fresh
P Giridhar et al.
Indian journal of experimental biology, 42(1), 106-110 (2004-07-28)
Axillary buds obtained from field grown plants of D. hamiltonii were used to initiate multiple shoots on Murashige and Skoog's medium (MS) supplemented with 2 mg L(-1) 6-benzyl aminopurine (BA) and 0.5 mg L(-1) indole-3-acetic acid (IAA). Profuse rooting was
Rubén Córdoba et al.
Bioorganic & medicinal chemistry, 15(15), 5300-5315 (2007-05-18)
A series of analogues of the potentially angiogenic inhibitor aeroplysinin-1 1 were synthesized and their in vitro antiangiogenic and cytotoxic activities evaluated. In the case of epoxy ketone 6 and azlactone 36 the relationship sprouting inhibition assay/cytotoxicity in BAE cells
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