Home Halogens Propanoic acid, 2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]-, (2R)-

Propanoic acid, 2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]-, (2R)-

CAS No.:
114420-56-3
Catalog Number:
AG000BBC
Molecular Formula:
C14H11ClFNO4
Molecular Weight:
311.6928
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Product Description
Catalog Number:
AG000BBC
Chemical Name:
Propanoic acid, 2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]-, (2R)-
CAS Number:
114420-56-3
Molecular Formula:
C14H11ClFNO4
Molecular Weight:
311.6928
MDL Number:
MFCD08273808
IUPAC Name:
(2R)-2-[4-(5-chloro-3-fluoropyridin-2-yl)oxyphenoxy]propanoic acid
InChI:
InChI=1S/C14H11ClFNO4/c1-8(14(18)19)20-10-2-4-11(5-3-10)21-13-12(16)6-9(15)7-17-13/h2-8H,1H3,(H,18,19)/t8-/m1/s1
InChI Key:
YUIKUTLBPMDDNQ-MRVPVSSYSA-N
SMILES:
OC(=O)[C@H](Oc1ccc(cc1)Oc1ncc(cc1F)Cl)C
EC Number:
601-312-5
UNII:
I5VL6U0SD8
Properties
Complexity:
352  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
311.036g/mol
Formal Charge:
0
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
311.693g/mol
Monoisotopic Mass:
311.036g/mol
Rotatable Bond Count:
5  
Topological Polar Surface Area:
68.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.4  
Literature
Title Journal
Waterborne exposure to clodinafop-propargyl disrupts the posterior and ventral development of zebrafish embryos. Environmental toxicology and chemistry 20110701
Phosphate-solubilizing and plant-growth-promoting Pseudomonas aeruginosa PS1 improves greengram performance in quizalafop-p-ethyl and clodinafop amended soil. Archives of environmental contamination and toxicology 20100201
Prevalence of cross- or multiple resistance to the acetyl-coenzyme A carboxylase inhibitors fenoxaprop, clodinafop and pinoxaden in black-grass (Alopecurus myosuroides Huds.) in France. Pest management science 20100201
Toxicity assessment of herbicides quizalafop-p-ethyl and clodinafop towards Rhizobium pea symbiosis. Bulletin of environmental contamination and toxicology 20090601
In vitro study of DNA interaction with clodinafop-propargyl herbicide. DNA and cell biology 20081001
Liquid chromatographic method for the micro-quantitative determination of clodinafop in soil, wheat and Phalaris minor. Journal of chromatography. A 20050218
Phototransformation of clodinafop-propargyl. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20050101
Clotrimazole, ketoconazole, and clodinafop-propargyl inhibit the in vitro growth of Babesia bigemina and Babesia bovis (Phylum Apicomplexa). Parasitology 20031001
Clotrimazole, ketoconazole, and clodinafop-propargyl as potent growth inhibitors of equine Babesia parasites during in vitro culture. The Journal of parasitology 20030601
Influence of application volume on herbicide efficacy. Communications in agricultural and applied biological sciences 20030101
PCR-based detection of resistance to acetyl-CoA carboxylase-inhibiting herbicides in black-grass (Alopecurus myosuroides Huds) and ryegrass (Lolium rigidum gaud). Pest management science 20020501
New, quick tests for herbicide resistance in black-grass (Alopecurus myosuroides Huds) based on increased glutathione S-transferase activity and abundance. Pest management science 20020101
Growth of Toxoplasma gondii is inhibited by aryloxyphenoxypropionate herbicides targeting acetyl-CoA carboxylase. Proceedings of the National Academy of Sciences of the United States of America 19991109
Properties