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Assay
97%
mp
202-207 °C (lit.)
SMILES string
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
Related Categories
General description
2-Bromo-3-hydroxy-4-methoxybenzaldehyde, also known as 2-bromo-isovanillin, can be synthesized by the bromination of 3-hydroxy-4-methoxybenzaldehyde.
Application
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Chemoselective Zinc/HCl Reduction of Halogenated β-Nitrostyrenes: Synthesis of Halogenated Dopamine Analogues.
Synlett, 25, 2891-2894 (2014)
A concise synthesis of denbinobin.
Tetrahedron Letters, 46(47), 8103-8104 (2005)
Concise syntheses of (-)-galanthamine and (?)-codeine via intramolecular alkylation of a phenol derivative.
Journal of the American Chemical Society, 131(44), 16045-16047 (2009)
Synthesis and preliminary biological evaluation of novel taspine derivatives as anticancer agents.
European Journal of Medicinal Chemistry, 45(7), 2798-2805 (2010)
Growth, spectral, and thermal characterization of 2-hydroxy-3-methoxybenzaldehyde semicarbazone.
Journal of Thermal Analysis and Calorimetry, 112(2), 913-919 (2013)
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