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Details

Stereochemistry ACHIRAL
Molecular Formula C8Cl2N2O2
Molecular Weight 227.004
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-DICHLORO-5,6-DICYANOBENZOQUINONE

SMILES

ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O

InChI

InChIKey=HZNVUJQVZSTENZ-UHFFFAOYSA-N
InChI=1S/C8Cl2N2O2/c9-5-6(10)8(14)4(2-12)3(1-11)7(5)13

HIDE SMILES / InChI
Molecular Formula C8Cl2N2O2
Molecular Weight 227.004
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
Preparations of heterospirostanols and their pharmacological activities.
2002 Aug
Determination of meloxicam in bulk and pharmaceutical formulations.
2003 Aug 21
Validated spectrophotometric methods for the determination of amlodipine besylate in drug formulations using 2,3-dichloro 5,6-dicyano 1,4-benzoquinone and ascorbic acid.
2003 Feb 26
Use of pi-acceptors for spectrophotometric determination of dicyclomine hydrochloride.
2003 Jan-Feb
Synthesis and supramolecular properties of trimethylene-bridged clips.
2003 Oct 17
Alpha-conidendrin as a source for preparation of sikkimotoxin derivatives.
2004 Apr
Self-aggregation of synthetic protobacteriochlorophyll-d derivatives.
2005 Jan-Feb
Spectrophotometric study of interaction of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone with diaza-18-crown-6 and diaza-15-crown-5 in acetonitrile and chloroform solutions.
2005 Mar
Spectrophotometric and electrical studies of charge transfer complexes of 2-amino-1,3,4-thiadiazole with pi-acceptors.
2005 Nov
Spectroscopic studies on [(DD18C6H2)(HPA)2](PA)2 and [(DD18C6H2)(DDQ)2](DDQH)2 formed in the reaction of N,N'-dibenzyl-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane with HPA and DDQ.
2005 Sep
Liquid chromatographic determination of malachite green and leucomalachite green (LMG) residues in salmon with in situ LMG oxidation.
2005 Sep-Oct
Spectrophotometric determination of rifampicin through chelate formation and charge transfer complexation in pharmaceutical preparation and biological fluids.
2006 Aug
New charge-transfer salts for reversible resistive memory switching.
2006 Dec
Spectrophotometric study of the reaction mechanism between DDQ as pi-acceptor and potassium iodate and flucloxacillin and dicloxacillin drugs and their determination in pure and in dosage forms.
2006 Sep
Chemoselective reduction of 1,4,6-cholestatrien-3-one and 1,4,6-androstatriene-3,17-dione by various hydride reagents.
2007 Apr
Charge-transfer interaction of aromatic thiols with 2,3-dichloro-5,6-dicyano-p-benzoquinone: spectral and quantum mechanical studies.
2007 Dec 6
Spectroscopic studies of charge transfer complexes between colchicine and some pi acceptors.
2007 Jul
Diastereoselective tetrahydropyrone synthesis through transition-metal-free oxidative carbon-hydrogen bond activation.
2008
Bay-area selective thermal [4+2] and [4+4] cycloaddition reactions of triply linked ZnII diporphyrin with o-xylylene.
2008
Ultrasound-assisted thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and DDQ.
2008 Apr
Biomimetic synthesis of xuxuarines Ealpha and Ebeta: structure revision of Rzedowskia bistriterpenoids.
2008 Feb 15
Utility of some pi-acceptors for spectrophotometric determination of gatifloxacin in pure form and in pharmaceutical preparations.
2008 Jan
Highly selective synthesis of the ring-B reduced chlorins by ferric chloride-mediated oxidation of bacteriochlorins: effects of the fused imide vs isocyclic ring on photophysical and electrochemical properties.
2008 Oct 29
Cross-dehydrogenative coupling (CDC): exploring C-C bond formations beyond functional group transformations.
2009 Feb 17
Cyclization reactions through DDQ-mediated vinyl oxazolidinone oxidation.
2009 Jul 16
Modified 26 and 28 pi hexaphyrins with five meso-links: optical, redox, and structural properties.
2009 Jun 2
Resistive molecular memories: influence of molecular parameters on the electrical bistability.
2009 May 13
Total synthesis of (+)-schweinfurthins B and E.
2009 Sep 18
Tuning the electronic structure and transport properties of graphene by noncovalent functionalization: effects of organic donor, acceptor and metal atoms.
2010 Feb 10
Patents

Patents

04022769
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04075223
1
04132726
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04186199
3
04327023
3
04361558
1
04371536
7
04414154
1
04495202
1
04581356
2
04680298
1
04698352
3
04820873
1
04954518
13
04968689
1
05010077
7
05021414
2
05169857
6
05241107
2
05405851
8
05410054
2
05418231
1
05480913
1
05519051
1
05532207
4
05561150
1
05589478
2
05635477
1
05719182
3
05763444
1
05780675
1
05922711
7
05929106
1
05932726
1
06022523
2
06063810
1
06103905
1
06110911
1
06121309
2
06204293
4
JP2002515909A
1
JPH02250868A
1
JPH05320165A
1
JPH06256283A
1
JPH08259825A
2
JPH0873443A
1
JPS5436251A
1
JPS5455511A
1
JPS5632535A
1
JPS5871980A
1
JPS6089472A
1
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:54:14 GMT 2023
Edited
by admin
on Sat Dec 16 03:54:14 GMT 2023
Record UNII
1H5KD39UH7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-DICHLORO-5,6-DICYANOBENZOQUINONE
MI  
Systematic Name English
4,5-DICHLORO-3,6-DIOXO-1,2-BENZENEDICARBONITRILE
Systematic Name English
2,3-DICHLORO-5,6-CYANO-1,4-BENZOQUINONE
Common Name English
5,6-DICHLORO-2,3-DICYANO-P-BENZOQUINONE
Common Name English
2,3-DICYANO-5,6-DICHLORO-1,4-BENZOQUINONE
Systematic Name English
DICHLORODICYANOBENZOQUINONE
Systematic Name English
2,3-DICHLORO-5,6-DICYANO-P-QUINONE
Common Name English
4,5-DICHLORO-3,6-DIOXO-1,4-CYCLOHEXADIENE-1,2-DICARBONITRILE
Systematic Name English
1,2-DICHLORO-4,5-DICYANO-P-BENZOQUINONE
Common Name English
DDQ
Common Name English
2,3-DICHLORO-5,6-DICYANOBENZOQUINONE [MI]
Common Name English
5,6-DICYANO-2,3-DICHLORO-P-BENZOQUINONE
Common Name English
2,3-DICHLORO-5,6-DICYANO-1,4-BENZOQUINONE
Systematic Name English
2,3-DICHLORODICYANO-P-BENZOQUINONE
Common Name English
2,3-DICYANO-5,6-DICHLOROBENZOQUINONE
Systematic Name English
DICHLORODICYANO-P-BENZOQUINONE
Common Name English
2,3-DICHLORO-5,6-DICYANOQUINONE
Common Name English
DICHLORODICYANOQUINONE
Common Name English
2,3-CHLORO-5,6-DICYANOQUINONE
Common Name English
DICHLORO-5,6-DICYANO-1,4-BENZOQUINONE
Systematic Name English
2,3-DICHLORO-5,6-DICYANO-P-BENZOQUINONE
Common Name English
NSC-401087
Code English
Code System Code Type Description
EPA CompTox
DTXSID7052577
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
DRUG BANK
DB15684
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-542-2
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
FDA UNII
1H5KD39UH7
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
NSC
401087
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
PUBCHEM
6775
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
CAS
84-58-2
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
WIKIPEDIA
Dichlorodicyanobenzoquinone
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
MERCK INDEX
m4342
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY Merck Index
RXCUI
2288812
Created by admin on Sat Dec 16 03:54:14 GMT 2023 , Edited by admin on Sat Dec 16 03:54:14 GMT 2023
PRIMARY
NIH
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