Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H2Cl4O2 |
Molecular Weight | 247.891 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1O
InChI
InChIKey=RRBMVWQICIXSEO-UHFFFAOYSA-N
InChI=1S/C6H2Cl4O2/c7-1-2(8)4(10)6(12)5(11)3(1)9/h11-12H
Molecular Formula | C6H2Cl4O2 |
Molecular Weight | 247.891 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
cis-chlorobenzene dihydrodiol dehydrogenase (TcbB) from Pseudomonas sp. strain P51, expressed in Escherichia coli DH5alpha(pTCB149), catalyzes enantioselective dehydrogenase reactions. | 1999 Dec |
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Acute toxicity of (chloro-)catechols and (chloro-)catechol-copper combinations in Escherichia coli corresponds to their membrane toxicity in vitro. | 2001 Feb |
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Characterization of catechol glucuronidation in rat liver. | 2002 Feb |
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4,5,6,7-Tetrachlorobenzo[d][1,3,2]dioxaborol- 2-ol as an effective catalyst for the amide condensation of sterically demanding carboxylic acids. | 2006 Mar 30 |
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Iron(III)-catecholato complexes as structural and functional models of the intradiol-cleaving catechol dioxygenases. | 2007 Oct 1 |
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Rapid photocatalytic destruction of pentachlorophenol in F-Si-comodified TiO(2) suspensions under microwave irradiation. | 2009 Jan 30 |
|
Pentachlorophenol and its derivatives induce oxidative damage and morphological changes in human lymphocytes (in vitro). | 2010 May |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:46:59 GMT 2023
by
admin
on
Fri Dec 15 17:46:59 GMT 2023
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Record UNII |
5REG09UJO0
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Record Status |
Validated (UNII)
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Record Version |
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