Home Halogens Quinoline, 5,7-dichloro-4-(4-fluorophenoxy)-

Quinoline, 5,7-dichloro-4-(4-fluorophenoxy)-

CAS No.:
124495-18-7
Catalog Number:
AG000M4E
Molecular Formula:
C15H8Cl2FNO
Molecular Weight:
308.1345
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
200mg
>98.0%(GC)
1 week
United States
$217
- +
Product Description
Catalog Number:
AG000M4E
Chemical Name:
Quinoline, 5,7-dichloro-4-(4-fluorophenoxy)-
CAS Number:
124495-18-7
Molecular Formula:
C15H8Cl2FNO
Molecular Weight:
308.1345
MDL Number:
MFCD03265638
IUPAC Name:
5,7-dichloro-4-(4-fluorophenoxy)quinoline
InChI:
InChI=1S/C15H8Cl2FNO/c16-9-7-12(17)15-13(8-9)19-6-5-14(15)20-11-3-1-10(18)2-4-11/h1-8H
InChI Key:
WRPIRSINYZBGPK-UHFFFAOYSA-N
SMILES:
Fc1ccc(cc1)Oc1ccnc2c1c(Cl)cc(c2)Cl
UNII:
PPC78J1VCW
Properties
Complexity:
325  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
306.997g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
308.133g/mol
Monoisotopic Mass:
306.997g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
22.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.1  
Literature
Title Journal
A concentration addition model to assess activation of the pregnane X receptor (PXR) by pesticide mixtures found in the French diet. Toxicological sciences : an official journal of the Society of Toxicology 20140901
Environmental impact on vascular development predicted by high-throughput screening. Environmental health perspectives 20111101
Widely used pesticides with previously unknown endocrine activity revealed as in vitro antiandrogens. Environmental health perspectives 20110601
A Bayesian approach to assessing the uncertainty in estimating bioconcentration factors in earthworms--the example of quinoxyfen. Pest management science 20110601
Efficacy of fungicides with various modes of action in controlling the early stages of an Erysiphe necator-induced epidemic. Pest management science 20101201
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program. Chemical research in toxicology 20100315
Influence of several fungicides on the antioxidant activity of red wines (var. Monastrell). Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 20090801
[Determination of quinoxyfen residue in foodstuffs of plant and animal origins by high performance liquid chromatography]. Se pu = Chinese journal of chromatography 20080701
Host perception and signal transduction studies in wild-type Blumeria graminis f. sp. hordei and a quinoxyfen-resistant mutant implicate quinoxyfen in the inhibition of serine esterase activity. Pest management science 20080501
Suitability of two laboratory testing methods to evaluate the side effects of pesticides on Typhlodromus pyri Scheuten (Acari: Phytoseiidae). Pest management science 20080201
Pesticide volatilization from plants: improvement of the PEC model PELMO based on a boundary-layer concept. Environmental science & technology 20040515
Influence of different mineral and Organic pesticide treatments on Cd(II), Cu(II), Pb(II), and Zn(II) contents determined by derivative potentiometric stripping analysis in Italian white and red wines. Journal of agricultural and food chemistry 20030212
Occupational allergic contact dermatitis caused by 5,7-dichloro-4-(4-fluorophenoxy)quinoline (quinoxyfen). Contact dermatitis 20010801
Properties