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122008-82-6,MFCD09832888
Catalog No.:AA0016J9

122008-82-6 | Propanoic acid, 2-[4-(4-cyano-2-fluorophenoxy)phenoxy]-, butyl ester

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100mg
97%
2 weeks  
$255.00   $179.00
- +
250mg
97%
2 weeks  
$400.00   $280.00
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1g
97%
2 weeks  
$1,005.00   $704.00
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  • Technical Information
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA0016J9
Chemical Name:
Propanoic acid, 2-[4-(4-cyano-2-fluorophenoxy)phenoxy]-, butyl ester
CAS Number:
122008-82-6
Molecular Formula:
C20H20FNO4
Molecular Weight:
357.3755
MDL Number:
MFCD09832888
SMILES:
CCCCOC(=O)C(Oc1ccc(cc1)Oc1ccc(cc1F)C#N)C
Properties
Computed Properties
 
Complexity:
483  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
6  
Rotatable Bond Count:
9  
Undefined Atom Stereocenter Count:
1  
XLogP3:
4.8  

Literature

Title: Evaluation of harvest residues of Cyhalofop-butyl in paddy soil.

Journal: Bulletin of environmental contamination and toxicology 20120801

Title: Novel and highly effective chemoenzymatic synthesis of (2R)-2-[4-(4-cyano-2-fluorophenoxy)phenoxy]butylpropanoate based on lipase mediated transesterification.

Journal: Biotechnology letters 20120401

Title: Effects of sewage sludge amendments on pesticide sorption and leaching through undisturbed Mediterranean soils.

Journal: Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20120101

Title: Isolation of the fenoxaprop-ethyl (FE)-degrading bacterium Rhodococcus sp. T1, and cloning of FE hydrolase gene feh.

Journal: FEMS microbiology letters 20111001

Title: Degradation of cyhalofop-butyl (CyB) by Pseudomonas azotoformans strain QDZ-1 and cloning of a novel gene encoding CyB-hydrolyzing esterase.

Journal: Journal of agricultural and food chemistry 20110608

Title: Direct and indirect photolysis of cyhalofop in aqueous systems.

Journal: Chemosphere 20110201

Title: A multi-residue method for pesticide residue analysis in rice grains using matrix solid-phase dispersion extraction and high-performance liquid chromatography-diode array detection.

Journal: Analytical and bioanalytical chemistry 20100701

Title: Differential oxidative metabolism and 5-ketoclomazone accumulation are involved in Echinochloa phyllopogon resistance to clomazone.

Journal: Plant physiology 20100501

Title: Hydrolysis and adsorption of cyhalofop-butyl and cyhalofop-acid on soil colloids.

Journal: Journal of agricultural and food chemistry 20080709

Title: Effect of undesalted dissolved organic matter from composts on persistence, adsorption, and mobility of cyhalofop herbicide in soils.

Journal: Journal of agricultural and food chemistry 20080611

Title: Morphological and molecular characterization of different Echinochloa spp. and Oryza sativa populations.

Journal: Journal of agricultural and food chemistry 20060222

Title: Basis of selectivity of cyhalofop-butyl in Oryza sativa L.

Journal: Planta 20060101

Title: Determination of antagonism between cyhalofop-butyl and other rice (Oryza sativa) herbicides in barnyardgrass (Echinochloa crus-galli).

Journal: Journal of agricultural and food chemistry 20050518

Title: Is it possible to detect Echinochloa spp. tolerance to ACCase-inhibiting herbicides using a simple quick tolerance test?

Journal: Communications in agricultural and applied biological sciences 20030101

Title: Cross-resistance to ACCase inhibitors of Lolium multiflorum, Lolium perenne and Lolium rigidum found in Chile.

Journal: Communications in agricultural and applied biological sciences 20030101

Title: Alternative control of two biotypes of Echinochloa phyllopogon susceptible and resistant to fenoxaprop-ethyl.

Journal: Communications in agricultural and applied biological sciences 20030101

Title: Botanical identification of several Echinochloa biotypes collected in Spanish rice fields with control failures of cyhalofop-butyl.

Journal: Communications in agricultural and applied biological sciences 20030101

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Tags:122008-82-6 Molecular Formula|122008-82-6 MDL|122008-82-6 SMILES|122008-82-6 Propanoic acid, 2-[4-(4-cyano-2-fluorophenoxy)phenoxy]-, butyl ester