| Identification | Back Directory | [Name]
CLORANSULAM-METHYL | [CAS]
147150-35-4 | [Synonyms]
xde-565
CLORANSULAM-METHYL
ChloransulaM-Methyl
cloransulam-methyl (bsi, pa iso, ansi)
Methyl 3-chloro-N-(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-ylsulfonyl)anthranilate
Methyl 3-chloro-2-[(5-ethoxy-7-fluoro-[1,2,4]triazolo[5,1-c]pyrimidin-2-yl)sulfonylamino]benzoate
Methyl 3-chloro-2-{[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2-yl)sulfonyl]amino}benzoate
3-Chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]benzoic acid, Methyl ester | [EINECS(EC#)]
405-090-9 | [Molecular Formula]
C15H13ClFN5O5S | [MDL Number]
MFCD08273840 | [MOL File]
147150-35-4.mol | [Molecular Weight]
429.81 |
| Hazard Information | Back Directory | [Definition]
ChEBI: The methyl ester of cloransulam. An inhibitor of acetohydroxyacid synthase (AHAS), it prevents the synthesis of amino acids in plants and is used as a herbicide for the control of post-emergence control of broad-leaved weeds in soybeans. It is not approved
for use within the European Area. | [Metabolic pathway]
When 14C-cloransulam methyl is incubated with soils,
the degradation proceeds via the hydrolysis of the
ester group and O-de-ethylation on the
triazolopyrimidine ring to yield the three identified
metabolites, cloransulam, 5-hydroxycloransulam
methyl, and 5-hydroxycloransulam. These metabolites
are significantly less phytotoxic than the parent
herbicide. |
|
|