C85409
Coumalic acid
97%
Synonym(s):
2-Oxo-2H-pyran-5-carboxylic acid, 2-Pyrone-5-carboxylic acid
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About This Item
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Quality Level
Assay
97%
form
powder
bp
218 °C/120 mmHg (lit.)
mp
203-205 °C (dec.) (lit.)
SMILES string
OC(=O)C1=COC(=O)C=C1
InChI
1S/C6H4O4/c7-5-2-1-4(3-10-5)6(8)9/h1-3H,(H,8,9)
InChI key
ORGPJDKNYMVLFL-UHFFFAOYSA-N
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General description
Decarboxylates to α-pyrone, a Diels-Alder diene.
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
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Some chemicals were examined for their effects on the germination of resting spores of the clubroot pathogen Plasmodiophora brassicae, and on the control of clubroots in Chinese cabbage. Caffeic acid, coumalic acid, and corilagin stimulated the germination of Plasmodiophora spores
The Biochemical journal, 242(1), 163-169 (1987-02-15)
From the structure-activity relationships of known competitive inhibitors, coumalic acid (2-oxo-1,2H-pyran-5-carboxylic acid) was deduced to be a potential syncatalytic inhibitor for chick-embryo prolyl 4-hydroxylase. The compound caused time-dependent inactivation, the reaction rate being first-order. The inactivation constant was 0.094 min-1
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