质量水平
检测方案
97%
mp
202-207 °C (lit.)
SMILES字符串
COc1ccc(C=O)c(Br)c1O
InChI
1S/C8H7BrO3/c1-12-6-3-2-5(4-10)7(9)8(6)11/h2-4,11H,1H3
InChI key
QPDFBPIHEDAUKK-UHFFFAOYSA-N
一般描述
2-Bromo-3-hydroxy-4-methoxybenzaldehyde, also known as 2-bromo-isovanillin, can be synthesized by the bromination of 3-hydroxy-4-methoxybenzaldehyde.
应用
2-Bromo-3-hydroxy-4-methoxybenzaldehyde (2-Bromo-isovanillin) may be used in the preparation of:
- 2-hydroxy-3-methoxybenzaldehyde semicarbazone (HMBS)
- 2-cyclopentyl-7-methoxy-1-benzofuran-4-carbaldehyde
- 3-(benzyloxy)-2-bromo-4-methoxybenzaldehyde
- pareitropone
- denbinobin
- (±)-codeine
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
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
Total synthesis of pareitropone via radical anion coupling.
Organic Letters, 12(17), 3954-3956 (2010)
Concise syntheses of (-)-galanthamine and (?)-codeine via intramolecular alkylation of a phenol derivative.
Journal of the American Chemical Society, 131(44), 16045-16047 (2009)
Chemoselective Zinc/HCl Reduction of Halogenated β-Nitrostyrenes: Synthesis of Halogenated Dopamine Analogues.
Synlett, 25, 2891-2894 (2014)
Growth, spectral, and thermal characterization of 2-hydroxy-3-methoxybenzaldehyde semicarbazone.
Journal of Thermal Analysis and Calorimetry, 112(2), 913-919 (2013)
Synthesis and preliminary biological evaluation of novel taspine derivatives as anticancer agents.
European Journal of Medicinal Chemistry, 45(7), 2798-2805 (2010)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门