Introduction：Basic information about CLORANSULAM-METHYL CAS 147150-35-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
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 |
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CLORANSULAM-METHYL Chemical Properties
| Melting point | 216-218 °C |
| density | 1.538 g/cm3 |
| storage temp. | 0-6°C |
| pka | 3.97±0.50(Predicted) |
| BRN | 7501727 |
| InChI | InChI=1S/C15H13ClFN5O5S/c1-3-27-15-18-10(17)7-11-19-14(20-22(11)15)28(24,25)21-12-8(13(23)26-2)5-4-6-9(12)16/h4-7,21H,3H2,1-2H3 |
| InChIKey | BIKACRYIQSLICJ-UHFFFAOYSA-N |
| SMILES | C(OC)(=O)C1=CC=CC(Cl)=C1NS(C1N=C2C=C(F)N=C(OCC)N2N=1)(=O)=O |
| CAS DataBase Reference | 147150-35-4 |
| EPA Substance Registry System | Cloransulam-methyl (147150-35-4) |
Safety Information
| Hazard Codes | Xn,N |
| Risk Statements | 20-50 |
| Safety Statements | 61 |
| RIDADR | UN 3077 9 / PGIII |
| WGK Germany | 3 |
| Hazardous Substances Data | 147150-35-4(Hazardous Substances Data) |
CLORANSULAM-METHYL Usage And Synthesis
| Uses | Cloransulam-methyl is a triazolopyrimidine sulfonanilide herbicide. Cloransulam-methyl can be used to control broadleaf weeds in soybean by acetolactate synthase (ALS) inhibition[1]. |
| 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 approvedfor use within the European Area. |
| Metabolic pathway | When 14C-cloransulam methyl is incubated with soils,the degradation proceeds via the hydrolysis of theester group and O-de-ethylation on thetriazolopyrimidine ring to yield the three identifiedmetabolites, cloransulam, 5-hydroxycloransulammethyl, and 5-hydroxycloransulam. These metabolitesare significantly less phytotoxic than the parentherbicide. |
| References | [1] Jeffrey D. Wolt, et al. Products and Kinetics of Cloransulam-methyl Aerobic Soil Metabolism. J. Agric. Food Chem. 1996, 44, 1, 324-332. |
CLORANSULAM-METHYL Preparation Products And Raw materials
