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2,5-Dichloro-1,4-benzoquinone - >98.0%(HPLC), high purity , CAS No.615-93-0

    Grade & Purity:
  • ≥98%(HPLC)
In stock
Item Number
D154939
Grouped product items
SKU Size
Availability
Price Qty
D154939-200mg
200mg
2
$9.90
D154939-1g
1g
2
$30.90
D154939-5g
5g
1
$97.90
D154939-10g
10g
1
$176.90

Basic Description

Synonyms NSC 6251 | 2,5-Dichlorobenzo-1,4-quinone # | 2,5-Dichlorobenzoquinone | NSC6251 | SR-01000641767-1 | 2,5-Dichloro-1,4-benzoquinone, 98% | 2,5-Dichloro-2,5-cyclohexa-diene-1,4-dione | 2,4-dione, 2,5-dichloro- | D0343 | 2,5-Cyclohexadiene-1,4-dione, 2,5-dic
Specifications & Purity ≥98%(HPLC)
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbonyl compounds
Intermediate Tree Nodes Ketones - Cyclic ketones - Quinones - Benzoquinones
Direct Parent P-benzoquinones
Alternative Parents Vinylogous halides  Alpha-chloroketones  Vinyl chlorides  Chloroalkenes  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents P-benzoquinone - Alpha-haloketone - Alpha-chloroketone - Vinylogous halide - Chloroalkene - Haloalkene - Vinyl halide - Vinyl chloride - Organic oxide - Hydrocarbon derivative - Organochloride - Organohalogen compound - Aliphatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as p-benzoquinones. These are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively.
External Descriptors an organic chloride - a quinol

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504752239
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504752239
IUPAC Name 2,5-dichlorocyclohexa-2,5-diene-1,4-dione
INCHI InChI=1S/C6H2Cl2O2/c7-3-1-5(9)4(8)2-6(3)10/h1-2H
InChIKey LNXVNZRYYHFMEY-UHFFFAOYSA-N
Smiles C1=C(C(=O)C=C(C1=O)Cl)Cl
Isomeric SMILES C1=C(C(=O)C=C(C1=O)Cl)Cl
WGK Germany 3
RTECS DK3990000
Molecular Weight 176.98
Reaxy-Rn 1864206
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1864206&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number Certificate Type Date Item
G2426313 Certificate of Analysis Jul 22, 2024 D154939
G2426314 Certificate of Analysis Jul 22, 2024 D154939
G2426331 Certificate of Analysis Jul 22, 2024 D154939
G2426310 Certificate of Analysis Jul 22, 2024 D154939
G2426311 Certificate of Analysis Jul 22, 2024 D154939
G2426312 Certificate of Analysis Jul 22, 2024 D154939
B1927115 Certificate of Analysis Dec 12, 2022 D154939
I2209059 Certificate of Analysis Sep 14, 2022 D154939
C2225033 Certificate of Analysis Apr 30, 2022 D154939
F2229100 Certificate of Analysis Apr 30, 2022 D154939

Chemical and Physical Properties

Solubility Soluble in Methanol
Melt Point(°C) 160.0to164.0℃
Molecular Weight 176.980 g/mol
XLogP3 1.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 175.943 Da
Monoisotopic Mass 175.943 Da
Topological Polar Surface Area 34.100 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 235.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Bingwei Yang, Zhishuai Ye, Xiangyu Zhu, Rongchong Huang, Erqun Song, Yang Song.  (2023)  The redox activity of polychlorinated biphenyl quinone metabolite orchestrates its pro-atherosclerosis effect via CAV1 phosphorylation.  JOURNAL OF HAZARDOUS MATERIALS,  457  (131697). 
2. Chengyang Zhang, Guoyang Zhang, Jiyuan Jin, Hongcen Zheng, Zhiwei Zhou, Shujuan Zhang.  (2023)  Selenite-Catalyzed Reaction between Benzoquinone and Acetylacetone Deciphered the Enhanced Inhibition on Microcystis aeruginosa Growth.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,  57  (15): (6188–6195). 
3. Xiao Tu, Jiaxin Hu, Jinghao Peng, Qihan Chen, Yangle Zhao, Zemao Gu.  (2025)  Discovery of thymoquinone analogues with high anthelmintic activity against monogenean infections in goldfish (Carassius auratus).  VETERINARY PARASITOLOGY,  334  (110401). 

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