Recommended Products
Quality Level
Assay
97%
mp
81-84 °C (lit.)
SMILES string
COc1cc(Br)cc(C=O)c1OC
InChI
1S/C9H9BrO3/c1-12-8-4-7(10)3-6(5-11)9(8)13-2/h3-5H,1-2H3
InChI key
RVMWFOFQRYTRHZ-UHFFFAOYSA-N
Related Categories
General description
5-Bromo-2,3-dimethoxybenzaldehyde can be prepared by employing 5-bromo-2-hydroxy-3-methoxybenzaldehyde as a starting reagent.
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Flavonoids syntheses. V. Synthesis of flavonoids with three hydroxy and four methoxy groups and their spectral properties.
Chemical & Pharmaceutical Bulletin, 35(2), 660-667 (1987)
The cyclisation of benzylaminonitriles. Part 7. Regiospecific formation of methoxy-substituted isoquinolin-4-ones using methylthio activating groups.
Journal of the Chemical Society. Perkin Transactions 1, 3, 503-508 (1990)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service