- Cloransulam-methyl
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- $54.00 / 1mg
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2026-04-22
- CAS:147150-35-4
- Min. Order:
- Purity: 99.66%
- Supply Ability: 10g
- CLORANSULAM-METHYL
-
- $10.00 / 1KG
-
2026-03-20
- CAS:147150-35-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
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| | 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 |
| Melting point | 216-218 °C | | density | 1.538 g/cm3 | | storage temp. | 0-6°C | | pka | 3.97±0.50(Predicted) | | BRN | 7501727 | | Henry's Law Constant | 1.6×1011 mol/(m3Pa) at 25℃, Ebert et al. (2023) | | 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) |
| | 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 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. | | 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 |
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