Home Carboxys 7-Chloro-3-methylquinoline-8-carboxylic acid

7-Chloro-3-methylquinoline-8-carboxylic acid

CAS No.:
90717-03-6
Catalog Number:
AG006MTN
Molecular Formula:
C11H8ClNO2
Molecular Weight:
221.6397
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Product Description
Catalog Number:
AG006MTN
Chemical Name:
7-Chloro-3-methylquinoline-8-carboxylic acid
CAS Number:
90717-03-6
Molecular Formula:
C11H8ClNO2
Molecular Weight:
221.6397
MDL Number:
MFCD00145199
IUPAC Name:
7-chloro-3-methylquinoline-8-carboxylic acid
InChI:
InChI=1S/C11H8ClNO2/c1-6-4-7-2-3-8(12)9(11(14)15)10(7)13-5-6/h2-5H,1H3,(H,14,15)
InChI Key:
ALZOLUNSQWINIR-UHFFFAOYSA-N
SMILES:
Cc1cnc2c(c1)ccc(c2C(=O)O)Cl
UNII:
0OFY83UPMH
Properties
Complexity:
259  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
221.024g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
221.64g/mol
Monoisotopic Mass:
221.024g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
50.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.7  
Literature
Title Journal
Direct and indirect photolysis of two quinolinecarboxylic herbicides in aqueous systems. Chemosphere 20120201
Pesticide pressure and fish farming in barrage pond in Northeastern France Part I: site characterization and water quality. Environmental science and pollution research international 20110801
Simultaneous determination of pesticides, biopesticides and mycotoxins in organic products applying a quick, easy, cheap, effective, rugged and safe extraction procedure and ultra-high performance liquid chromatography-tandem mass spectrometry. Journal of chromatography. A 20110318
Feasibility Assessment of Micro-Electrode Chip Assay as a Method of Detecting Neurotoxicity in vitro. Frontiers in neuroengineering 20110101
Sorption-desorption of ionogenic compounds at the mineral-water interface: study of metal oxide-rich soils and pure-phase minerals. Environmental science & technology 20020201
Auxin herbicides induce H(2)O(2) overproduction and tissue damage in cleavers (Galium aparine L.). Journal of experimental botany 20010901
Properties