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flamprop-m-methyl

flamprop-m-methyl Suppliers list
Company Name: Alta Scientific Co., Ltd.  
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Products Intro: Product Name:Flamprop-M-methyl
CAS:63729-98-6
Purity:99% Package:10mg;100mg;1g
Company Name: Shenzhen Polymeri Biochemical Technology Co., Ltd.  
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Products Intro: Product Name:Flamprop-M-Methyl
CAS:63729-98-6
Company Name: TCI (Shanghai) Chemical Trading Co., Ltd.  
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Products Intro: Product Name:Flamprop-M-Methyl
CAS:63729-98-6
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Products Intro: CAS:63729-98-6
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
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Products Intro: Product Name:Flamprop-M-Methyl
CAS:63729-98-6
Purity:95%+
flamprop-m-methyl Basic information
Product Name:flamprop-m-methyl
Synonyms:wl 43423;methyl (2R)-2-[benzoyl-(3-chloro-4-fluoro-phenyl)amino]propanoate;(R)-2-(N-Benzoyl-3-chloro-4-fluoroanilino)propionic acid methyl ester;(R)-Flamprop-methyl;D-Mataven;N-Benzoyl-N-(3-chloro-4-fluorophenyl)-D-alanine methyl ester;D-Alanine, N-benzoyl-N-(3-chloro-4-fluorophenyl)-, methyl ester;Fenfuram Impurity 18
CAS:63729-98-6
MF:C17H15ClFNO3
MW:335.76
EINECS:
Product Categories:
Mol File:63729-98-6.mol
flamprop-m-methyl Structure
flamprop-m-methyl Chemical Properties
Melting point 85 °C
Boiling point 459.5±45.0 °C(Predicted)
density 1.309±0.06 g/cm3(Predicted)
pka-1.04±0.50(Predicted)
EPA Substance Registry SystemD-Alanine, N-benzoyl-N-(3-chloro-4-fluorophenyl)-, methyl ester (63729-98-6)
Safety Information
MSDS Information
flamprop-m-methyl Usage And Synthesis
Chemical PropertiesPurity of the original drug ≥ 96%, its pure product is white to gray crystals, melting point 84 ~ 86 ℃. Vapor pressure 1.0mPa(20℃). Distribution coefficient KowlgP=3.0. relative density 1.311(22℃). Solubility in water 0.016mg/L(25℃);Solubility in other solvents(g/L,25℃):acetone 406,n-alkane 2.3.Stable to light,heat and pH2-7. Hydrolyzed to acid and methanol in alkaline (pH>7).
Production MethodsFlamprop M methyl was produced through a straightforward aryloxyphenoxypropionate assembly, beginning with preparation of the chiral (M)-configured propionate intermediate, typically obtained either by resolution of a racemate or by using an enantioselective catalyst during ester formation. This intermediate was then coupled with the appropriate substituted anilide or phenoxy precursor via controlled esterification or acylation to build the herbicidally active structure. Manufacturers focused on maintaining stereochemical integrity, achieving clean conversion in the coupling step, and purifying the resulting ester to technical grade with tight control of impurities.
Mechanism of actionSelective, systemic, absorbed by leaves
Pesticide TypeHerbicide
flamprop-m-methyl Preparation Products And Raw materials
Tag:flamprop-m-methyl(63729-98-6) Related Product Information
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