CLORANSULAM-METHYL
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
- 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
- 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 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.
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CLORANSULAM-METHYL(147150-35-4)Related Product Information
- MCPA SODIUM
- Quizalofop-p-ethyl
- theta-Cypermethrin
- Flumetsulam
- Penoxsulam
- PYROXSULAM
- FLORASULAM
- DICLOSULAM
- CLORANSULAM-METHYL SOLUTION 100UG/ML IN ACETONITRILE 1ML
- CLORANSULAM-METHYL SOLUTION 100UG/ML IN TOLUENE 1ML
- [1,2,4]TRIAZOLO[1,5-C]PYRIMIDIN-5-OL
- Methyl 2-amino-3-chlorobenzoate
- CLORANSULAM-DESETHYL
- O-METHYLISOUREA ACETATE
- CLORANSULAM-METHYL