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Chloranilic acid

Chloranilic acid structure

Chloranilic acid 

structure
  • CAS No:

    87-88-7

  • Formula:

    C6H2Cl2O4

  • Chemical Name:

    Chloranilic acid

  • Synonyms:

    2,5-Cyclohexadiene-1,4-dione,2,5-dichloro-3,6-dihydroxy-;p-Benzoquinone,2,5-dichloro-3,6-dihydroxy-;Quinone,2,5-dichloro-3,6-dihydroxy-;2,5-Dichloro-3,6-dihydroxy-2,5-cyclohexadiene-1,4-dione;Chloranilic acid;2,5-Dichloro-3,6-dihydroxy-p-benzoquinone;2,5-Dichloro-3,6-dihydroxy-1,4-quinone;2,5-Dihydroxy-3,6-dichloro-1,4-benzoquinone;2,5-Dihydroxy-3,6-dichlorobenzoquinone;3,6-Dichloro-2,5-dihydroxy-1,4-benzoquinone;2,5-Dichloro-3,6-dihydroxy-1,4-benzoquinone;p-Chloranilic acid;NSC 6108;NSC 97383;3,6-Dichloro-2,5-dihydroxybenzoquinone;260353-37-5

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

orange or red crystals or powder

Chloranilic acid Basic Attributes

208.978

208.98

201-780-7

YJ8L3BB7Y4

6108

DTXSID3058959

2914700090

Characteristics

74.6

0.18

1.957 g/cm3

283.5 °C

300.3±42.0 °C at 760 mmHg

135.4±27.9 °C

1.655

Soluble in hot water and methanol. Insoluble in organic solvents.

Safety Information

NONH for all modes of transport

3

R36/37/38

S26-S36

DK4005000

Xi:Irritant;

Stable. Incompatible with strong oxidizing agents.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 53 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

2,5-dichloro-3,6-dihydroxy-p-benzoquinone

Chloranilic acid Use and Manufacturing

Uses

Chloranilic acid is the reactant involved in:• ;Acting as a proton donor in reactions studying dimensionality control1• ;Synthesis of dimethylbipyridyl complexes2• ;Synthesis of (nonylbenzimidazolylmethyl)benzene for preparation of neutral altitudinal rotor-shaped dirhenium metallacycles3• ;Charge-transfer reactions with metoprolol tartrate4• ;Salt formation with organic bases5• ;Synthesis of osmium metalla-rectangles with anticancer activity6 A benzoquinone derivative that inhibits camel lens ξ-crystallin/NADPH: quinone oxidoreductase activity. Potential antibacterial activities against methicillin-resistant Staphylococcus aureus. Reacts with metal cations to form stable salts. Used in spectrophotometry: Hart, organic. Chem. Bull. 33, no. 3 (1961).

2,5-Cyclohexadiene-1,4-dione, 2,5-dichloro-3,6-dihydroxy-: ACTIVE

Computed Properties

Molecular Weight:208.98
XLogP3:1.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Exact Mass:207.9330139
Monoisotopic Mass:207.9330139
Topological Polar Surface Area:74.6
Heavy Atom Count:12
Complexity:306
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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