Other grades of this product :
| CLORANSULAM-METHYL Basic information |
| Product Name: | CLORANSULAM-METHYL | | Synonyms: | Benzoic acid, 3-chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]-, methyl ester;CLORANSULAM-METHYL;cloransulam-methyl (bsi, pa iso, ansi);xde-565;Methyl 3-chloro-2-{[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine-2-yl)sulfonyl]amino}benzoate;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;3-Chloro-2-[[(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidin-2-yl)sulfonyl]amino]benzoic acid, Methyl ester | | CAS: | 147150-35-4 | | MF: | C15H13ClFN5O5S | | MW: | 429.81 | | EINECS: | 405-090-9 | | Product Categories: | | Mol File: | 147150-35-4.mol |
| CLORANSULAM-METHYL Chemical Properties |
| CLORANSULAM-METHYL Usage And Synthesis |
| 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. |
| CLORANSULAM-METHYL Preparation Products And Raw materials |
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