189839
2,3-二羟基苯甲醛
97%
别名:
1,2-二羟基-3-甲酰苯, 3-甲酰基-1,2-苯二酚, 3-羟基水杨醛, 5,6-二羟基苯甲醛
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关于此项目
线性分子式:
(HO)2C6H3CHO
化学文摘社编号:
分子量:
138.12
Beilstein:
2041781
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
97%
mp
104-108 °C (lit.)
溶解性
95% ethanol: soluble 50 mg/mL, clear, colorless to greenish-yellow
官能团
aldehyde
SMILES字符串
[H]C(=O)c1cccc(O)c1O
InChI
1S/C7H6O3/c8-4-5-2-1-3-6(9)7(5)10/h1-4,9-10H
InChI key
IXWOUPGDGMCKGT-UHFFFAOYSA-N
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一般描述
在不同pH值下甲醇中2,3-二羟基苯甲醛的电化学氧化已通过使用循环伏安法和受控电位库仑法进行了研究。
应用
2,3-二羟基苯甲醛已被用于合成席夫碱的铜（II）配合物。它也被用于合成2-乙氧基-3-羟基-4-硝基苯甲酸。
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
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M E Ramos-Nino et al.
Journal of applied microbiology, 84(2), 207-212 (1998-06-20)
Quantitative structure activity relationships (QSARs) were obtained describing the activity of a series of benzaldehydes against three different foodborne bacteria, Listeria monocytogenes F6861, serotype 4b, Salmonella enteritidis, Phage type 4, P167807 and Lactobacillus plantarum INT.L11. MIC values at pH 6.2
Investigation of the Electromethoxylation Reaction Part 2: Electrochemical Study of 3-Methylcatechol and 2, 3-Dihydroxybenzaldehyde in Methanol.
Nematollahi D and Golabi SM.
Electroanalysis, 13(12), 1008-1015 (2001)
S Kato et al.
Chemical & pharmaceutical bulletin, 44(8), 1484-1492 (1996-08-01)
To confirm the proposed structures of the minor metabolites of a potential gastroprokinetic agent, mosapride, 4-amino-5-chloro-2-ethoxy-3-hydroxy-N-(2-morpholinylmethyl)benzamide (3) and the N-(5-oxo-2-morpholinyl)-methyl analogue 4 were prepared. As the common intermediate, 2-ethoxy-3-hydroxy-4-nitrobenzoic acid (15) was prepared via the regioselective ethylation of 2,3-dihydroxybenzaldehyde (10)
Jong H Kim et al.
FEMS microbiology letters, 281(1), 64-72 (2008-02-21)
Activities of conventional antifungal agents, fludioxonil, strobilurin and antimycin A, which target the oxidative and osmotic stress response systems, were elevated by coapplication of certain benzo analogs (aldehydes and acids). Fungal tolerance to 2,3-dihydroxybenzaldehyde or 2,3-dihydroxybenzoic acid was found to
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