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π§ͺ 5-Chloro-2-oxopent-4-enoate
Appears in:
1 pathway
Produces:
1 compound
Produced by:
2 transformations
Chemical Structure
π Properties
SMILES:
O=C([O-])C(=O)CC=CCl
InChI:
InChI=1S/C5H5ClO3/c6-3-1-2-4(7)5(8)9/h1,3H,2H2,(H,8,9)/p-1/b3-1+
Database ID:
631
External:
View on PubChem β
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π¬ Reactant
5-Chloro-2-oxopent-4-enoate
β
5-Chloro-4-hydroxy-2-oxopentanate
5-Chloro-2-oxopent-4-enoate hydratase
(Eawag BBD reaction r1436)
(EC 4.2.1.-)
In pathway:
2,4-Dichlorophenoxyacetic Acid
π¬ Product
5-Chloro-2-hydroxymuconate
β
5-Chloro-2-oxopent-4-enoate
4-oxalocrotonate decarboxylase
(Eawag BBD reaction r1435)
(EC 4.1.1.77)
In pathway:
2,4-Dichlorophenoxyacetic Acid
5-Chloro-2-hydroxymuconic semialdehyde
β
5-Chloro-2-oxopent-4-enoate
2-hydroxymuconate semialdehyde hydrolase
(Eawag BBD reaction r0289)
(EC 3.7.1.9)
In pathway:
2,4-Dichlorophenoxyacetic Acid
πΊοΈ All Pathways Containing This Compound
2,4-Dichlorophenoxyacetic Acid
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