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π§ͺ Alachlor
Appears in:
1 pathway
Produces:
5 compounds
Chemical Structure
π Properties
SMILES:
O=C(N(C=1C(=CC=CC1CC)CC)COC)CCl
InChI:
InChI=1S/C14H20ClNO2/c1-4-11-7-6-8-12(5-2)14(11)16(10-18-3)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3
Database ID:
725
External:
View on PubChem β
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π
Starting Compound:
This compound serves as the root (starting point) for 1 degradation pathway.
π¬ Reactant
Alachlor
β
2-Hydroxy-2`,6`-diethyl-N-acetanilide
Eawag BBD reaction r1693
In pathway:
Alachlor
Alachlor
β
2-Chloro-2`,6`-diethylacetanilide
alachlor hydrolase
(Eawag BBD reaction r1677)
(EC 3.3.2.-)
In pathway:
Alachlor
Alachlor
β
Formaldehyde
alachlor hydrolase
(Eawag BBD reaction r1677)
(EC 3.3.2.-)
In pathway:
Alachlor
Alachlor
β
2,6-Diethyl-N-(methoxymethyl)aniline
alachlor amidohydrolase
(Eawag BBD reaction r1696)
(EC 3.5.1.-)
In pathway:
Alachlor
Alachlor
β
Chloroacetate
alachlor amidohydrolase
(Eawag BBD reaction r1696)
(EC 3.5.1.-)
In pathway:
Alachlor
πΊοΈ All Pathways Containing This Compound
Alachlor
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