所有图片(1)
About This Item
线性分子式:
HOC6H2(OCH3)2CHO
CAS号:
分子量:
182.17
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案
95%
mp
225 °C (dec.) (lit.)
官能团
aldehyde
SMILES字符串
COc1cc(O)cc(OC)c1C=O
InChI
1S/C9H10O4/c1-12-8-3-6(11)4-9(13-2)7(8)5-10/h3-5,11H,1-2H3
InChI key
HZWPJAZIRZFCGX-UHFFFAOYSA-N
一般描述
2,6-Dimethoxy-4-hydroxybenzaldehyde (4-hydroxy-2,6-dimethoxybenzaldehyde) is a p-hydroxybenzaldehyde derivative. Its synthesis by Vielsmeyer-Haack reaction and confirmation of the product formation by 1H NMR has been reported. Its structure has been investigated. The sodium salt of 4-hydroxy-2,6-dimethoxybenzaldehyde may be used to derivatize Merrifield resin to form resin-bound aldehyde.
应用
2,6-Dimethoxy-4-hydroxybenzaldehyde (4-hydroxy-2,6-dimethoxybenzaldehyde) may be used as a test compound to investigate the bactericidal activity of benzaldehydes against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes and Salmonella enterica.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Mendel Friedman et al.
Journal of food protection, 66(10), 1811-1821 (2003-10-24)
We evaluated the bactericidal activities of 35 benzaldehydes, 34 benzoic acids, and 1 benzoic acid methyl ester against Campylobacter jejuni, Escherichia coli O157:H7, Listeria monocytogenes, and Salmonella enterica when these compounds were substituted on the benzene ring with 0, 1
A Structure-Based Activation Model of Phenol-Receptor Protein Interactions.
Lee K.
Bull. Korean Chem. Soc., 18, 16-22 (1997)
4-Hydroxy-2, 6-dimethoxybenzaldehyde.
Wuyts C, et al.
Acta Crystallographica Section E, Structure Reports Online, 61(1), 79-80 (2004)
Ming-Fu Cheng et al.
Journal of combinatorial chemistry, 6(1), 99-104 (2004-01-13)
A library of 1,4-benzodiazepine-2,5-dione dicarboxylate derivatives containing aryl substituents at N(1)- and N(4)-positions to mimic the amino acid residues of Try-13, Phe-14, and Asp-18 in endothelin-1 is established by using the starting materials of alpha-amino esters, hydroxybenzaldehydes, nitrobenzoyl chlorides, and
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