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Quality Level
Assay
97%
mp
126-130 °C (lit.)
SMILES string
[H]C(=O)C1=C(Cl)c2ccccc2OC1=O
InChI
1S/C10H5ClO3/c11-9-6-3-1-2-4-8(6)14-10(13)7(9)5-12/h1-5H
InChI key
CLLLQUGVEQADNN-UHFFFAOYSA-N
General description
4-Chloro-3-formylcoumarin, also known as 4-chloro-2-oxo-2H-chromene-3-carbaldehyde, is a coumarin derivative.
Application
4-Chloro-3-formylcoumarin may be used as a reactant in the preparation of:
- 2-aryl[1]benzopyrano[4,3-c]pyrazol-4(2H)-ones
- biaryl lactones (benzo[c]chromen-6-ones)
- N-monosubstituted 4-amino-3-formylcoumarins
- chromeno[4,3-b]quinolin-6-one
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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Customers Also Viewed
Reactions of 4-Chloro-3-formylcoumarin with Arylhydrazines.
Chemistry of Heterocyclic Compounds, 39(12), 1608-1616 (2003)
One-Pot Synthesis of Biaryl Lactones by Sonogashira Cross-Coupling Reactions of 4-Chloro-3-formylcoumarin and Subsequent Domino [5+1] Cyclization/Deacetylation Reactions with 1, 3-Dicarbonyl Compounds.
Advanced Synthesis & Catalysis, 354(5), 803-806 (2012)
Reactions of 4-chloro-3-formyl-coumarin with primary amines.
Chemistry of Heterocyclic Compounds, 42(5), 574-582 (2006)
An efficient ultrasound promoted catalyst-free protocol for the synthesis of chromeno [4,3-b] quinolin-6-ones.
Chemical Science, 123(5), Prasad JV-Prasad JV (2011)
Synthesis of 6H-benzo [c] chromen-6-ones by cyclocondensation of 1,3-dicarbonyl compounds with 4-chloro-3-formylcoumarin.
Tetrahedron Letters, 52(45), 5910-5912 (2011)
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