Home Halogens 3,5-Dichlorocatechol

3,5-Dichlorocatechol

CAS No.:
13673-92-2
Catalog Number:
AG003ILU
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG003ILU
Chemical Name:
3,5-Dichlorocatechol
CAS Number:
13673-92-2
MDL Number:
MFCD02683889
IUPAC Name:
3,5-dichlorobenzene-1,2-diol
InChI:
InChI=1S/C6H4Cl2O2/c7-3-1-4(8)6(10)5(9)2-3/h1-2,9-10H
InChI Key:
XSXYVLIPQMXCBV-UHFFFAOYSA-N
Properties
Complexity:
120  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
177.959g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
178.996g/mol
Monoisotopic Mass:
177.959g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.7  
Literature
Title Journal
Catechol 1,2-dioxygenase from the Gram-positive Rhodococcus opacus 1CP: quantitative structure/activity relationship and the crystal structures of native enzyme and catechols adducts. Journal of structural biology 20100601
Induction of enzymes of 2,4-dichlorophenoxyacetate degradation in Burkholderia cepacia 2a and toxicity of metabolic intermediates. Biodegradation 20080901
Transformation of phenolic compounds upon UVA irradiation of anthraquinone-2-sulfonate. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20080301
Carbon suboxide, a highly reactive intermediate from the abiotic degradation of aromatic compounds in soil. Environmental science & technology 20071115
Pseudomonas putida KT2440 responds specifically to chlorophenoxy herbicides and their initial metabolites. Proteomics 20060601
Phylogenetical approach to isolation of white-rot fungi capable of degrading polychlorinated dibenzo-p-dioxin. Applied microbiology and biotechnology 20051201
Two kinds of chlorocatechol 1,2-dioxygenase from 2,4-dichlorophenoxyacetate-degrading Sphingomonas sp. strain TFD44. Biochemical and biophysical research communications 20050715
Two unusual chlorocatechol catabolic gene clusters in Sphingomonas sp. TFD44. Archives of microbiology 20050201
A linear megaplasmid, p1CP, carrying the genes for chlorocatechol catabolism of Rhodococcus opacus 1CP. Microbiology (Reading, England) 20040901
Assimilatory detoxification of herbicides by Delftia acidovorans MC1: induction of two chlorocatechol 1,2-dioxygenases as a response to chemostress. Microbiology (Reading, England) 20020901
Analysis of oxidative degradation products of 2,4,6-trichlorophenol treated with air ions. Analytical chemistry 20010715
The chlorocatechol degradative genes, tfdT-CDEF, of Burkholderia sp. strain NK8 are involved in chlorobenzoate degradation and induced by chlorobenzoates and chlorocatechols. Gene 20010502
Acute toxicity of (chloro-)catechols and (chloro-)catechol-copper combinations in Escherichia coli corresponds to their membrane toxicity in vitro. Environmental toxicology and chemistry 20010201
Purification of 3,5-dichlorocatechol 1,2-dioxygenase, a nonheme iron dioxygenase and a key enzyme in the biodegradation of a herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D), from Pseudomonas cepacia CSV90. Archives of biochemistry and biophysics 19930201
Affinity purification and characterization of 2,4-dichlorophenol hydroxylase from Pseudomonas cepacia. Archives of biochemistry and biophysics 19910701
Properties