Home Halogens 2,6-Dichlorobenzoic acid

2,6-Dichlorobenzoic acid

CAS No.:
50-30-6
Catalog Number:
AG003G3A
Molecular Formula:
C7H4Cl2O2
Molecular Weight:
191.0115
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
97%
In Stock USA
United States
$13
- +
25g
97%
In Stock USA
United States
$19
- +
100g
97%
In Stock USA
United States
$50
- +
500g
97%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG003G3A
Chemical Name:
2,6-Dichlorobenzoic acid
CAS Number:
50-30-6
Molecular Formula:
C7H4Cl2O2
Molecular Weight:
191.0115
MDL Number:
MFCD00002418
IUPAC Name:
2,6-dichlorobenzoic acid
InChI:
InChI=1S/C7H4Cl2O2/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3H,(H,10,11)
InChI Key:
MRUDNSFOFOQZDA-UHFFFAOYSA-N
SMILES:
OC(=O)c1c(Cl)cccc1Cl
EC Number:
200-025-9
UNII:
634RI764QT
NSC Number:
76599
Properties
Complexity:
151  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
189.959g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
191.007g/mol
Monoisotopic Mass:
189.959g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2  
Literature
Title Journal
Intermediate accumulation of metabolites results in a bottleneck for mineralisation of the herbicide metabolite 2,6-dichlorobenzamide (BAM) by Aminobacter spp. Applied microbiology and biotechnology 20120401
Determination of an ion exchange constant by the use of a kinetic probe: a new semiempirical kinetic approach involving the effects of 3-F- and 4-F-substituted benzoates on the rate of piperidinolysis of anionic phenyl salicylate in aqueous cationic micelles. Langmuir : the ACS journal of surfaces and colloids 20100706
Synthesis and evaluation of a novel series of quinoline derivatives with immunosuppressive activity. Bioorganic & medicinal chemistry 20090801
Determination of 2,6-dichlorobenzamide and its degradation products in water samples using solid-phase extraction followed by liquid chromatography-tandem mass spectrometry. Journal of chromatography. A 20090703
Mutational analysis of the inducer recognition sites of the LysR-type transcriptional regulator TfdT of Burkholderia sp. NK8. Applied microbiology and biotechnology 20090701
Mechanism of cis-dihydroxylation and epoxidation of alkenes by highly H(2)O(2) efficient dinuclear manganese catalysts. Inorganic chemistry 20070806
Microbial degradation pathways of the herbicide dichlobenil in soils with different history of dichlobenil-exposure. Environmental pollution (Barking, Essex : 1987) 20070701
Transformation of the herbicide 2,6-dichlorobenzonitrile to the persistent metabolite 2,6-dichlorobenzamide (BAM) by soil bacteria known to harbour nitrile hydratase or nitrilase. Biodegradation 20061201
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
GC-MS analysis of dichlobenil and its metabolites in groundwater. Talanta 20051115
Diversity of biphenyl degraders in a chlorobenzene polluted aquifer. Chemosphere 20050101
Solid-state structures of zinc(II) benzoate complexes. Catalyst precursors for the coupling of carbon dioxide and epoxides. Inorganic chemistry 20020225
Properties