C8136
Chloranilic acid
≥98%
Synonym(s):
2,5-Dichloro-3,6-dihydroxy-2,5-cyclohexadiene-1,4-dione, 2,5-Dichloro-3,6-dihydroxy-p-benzoquinone, NSC 6108, NSC 97383
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About This Item
Empirical Formula (Hill Notation):
C6H2Cl2O4
CAS Number:
Molecular Weight:
208.98
Beilstein:
1875040
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥98%
form
powder
mp
≥300 °C (lit.)
SMILES string
OC1=C(Cl)C(=O)C(O)=C(Cl)C1=O
InChI
1S/C6H2Cl2O4/c7-1-3(9)5(11)2(8)6(12)4(1)10/h9,12H
InChI key
IPPWILKGXFOXHO-UHFFFAOYSA-N
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Application
Reactant involved in:
- Acting as a proton donor in reactions studying dimensionality control
- Synthesis of dimethylbipyridyl complexes
- Synthesis of (nonylbenzimidazolylmethyl)benzene for preparation of neutral altitudinal rotor-shaped dirhenium metallacycles
- Charge-transfer reactions with metoprolol tartrate
- Salt formation with organic bases
- Synthesis of osmium metalla-rectangles with anticancer activity
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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M Walash et al.
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Two Spectrophotometric procedures are presented for the determination of two commonly used H2-receptor antagonists, nizatidine (I) and ranitidine hydrochloride (II). The methods are based mainly on charge transfer complexation reaction of these drugs with either p-chloranilic acid (rho-CA) or 2
Luis G Treviño-Quintanilla et al.
Journal of microbiology (Seoul, Korea), 49(6), 974-980 (2011-12-29)
Pentachlorophenol is the most toxic and recalcitrant chlorophenol because both aspects are directly proportional to the halogenation degree. Biological and abiotic pentachlorophenol degradation generates p-chloranil, which in neutral to lightly alkaline environmental conditions is hydrolyzed to chloranilic acid that present
Hydrogen bonding in two solid phases of phenazine-chloranilic acid (1/1) determined at 170 and 93 K.
Kazuma Gotoh et al.
Acta crystallographica. Section C, Crystal structure communications, 63(Pt 1), o17-o20 (2007-01-09)
The crystal structures in two solid phases, i.e. phase II stable between 146 and 253 K and phase IV below 136 K, of the title compound [phenazine-chloranilic acid (1/1), C12H8N2.C6H2Cl2O4, in phase II, and phenazinium hydrogen chloranilate, C12H9N2+.C6HCl2O4-, in phase
Pabitra Baran Chatterjee et al.
Inorganic chemistry, 48(3), 804-806 (2009-01-09)
In basic media, the coordinated semiquinone radical in the spin-coupled [(bipy)ClV(IV)O(TCSQ)] 1 (HTCSQ = tetrachlorosemiquinone) undergoes nucleophilic ipso substitution (OH- for Cl-) to generate the chloranilate anion (CA(2-)) that bridges the vanadium(IV) centers, forming a binuclear compound [(bipy)ClV(IV)O(CA)OV(IV)Cl(bipy)] 2.
B Palade et al.
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 114(1), 260-265 (2010-06-01)
In this paper we followed up the stability of ceftazidime, raw material used in drug industry. Matherials and methods: We used three spectrophotometric methods based on ceftazidime property to form complexes with p-chloranilic acid (ac. p-CA), 3-methylbenzothiazolin-2-on hydrazone (MBTH) and
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