CAS 87-88-7

Chloranilic acid

Description:

Chloranilic acid, with the CAS number 87-88-7, is an organic compound that belongs to the class of aromatic acids. It is characterized by its dark red to brown crystalline appearance and is known for its solubility in polar solvents such as water and alcohol. The chemical structure features a chlorinated aniline moiety, which contributes to its acidic properties and reactivity. Chloranilic acid is often used as a reagent in analytical chemistry, particularly in the determination of metal ions due to its ability to form colored complexes. Additionally, it exhibits properties that make it useful in dye synthesis and as a pH indicator. The compound is also noted for its potential applications in organic electronics and materials science. However, it should be handled with care, as it may pose health risks upon exposure. Overall, chloranilic acid is a versatile compound with significant utility in various chemical applications.

Formula: C₆H₂Cl₂O₄

InChI: InChI=1S/C6H2Cl2O4/c7-1-3(9)5(11)2(8)6(12)4(1)10/h9,12H

InChI key: InChIKey=IPPWILKGXFOXHO-UHFFFAOYSA-N

SMILES: ClC=1C(=O)C(O)=C(Cl)C(=O)C1O

Synonyms:

• 2,5-Cyclohexadiene-1,4-Dione, 2,5-Dichloro-3,6-Dihydroxy-
• 2,5-Dichloro-3,6-Dihydroxy-1,4-Benzoquinone
• 2,5-Dichloro-3,6-Dihydroxy-P-Benzoquinon
• 2,5-Dichloro-3,6-Dihydroxy-P-Benzoquinone
• 2,5-Dichloro-3,6-Dihydroxy-P-Quinon
• 2,5-Dichloro-3,6-Dihydroxy-P-Quinone
• 2,5-Dichloro-3,6-Dihydroxybenzo-1,4-Quinone
• 2,5-Dichloro-3,6-Dihydroxybenzoquinone
• 2,5-Dichloro-3,6-Dihydroxycyclohexa-2,5-Diene-1,4-Dione
• 2,5-Dichloro-3,6-Dihydroxyquinone
• 2,5-Dichloro-3,6-dihydroxy-1,4-quinone
• 2,5-Dichloro-3,6-dihydroxy-2,5-cyclohexadiene-1,4-dione
• 2,5-Dihydroxy-3,6-Dichlorobenzoquinone
• 2,5-Dihydroxy-3,6-dichloro-1,4-benzoquinone
• 2,5-Dochloro-3,6-Dihydroxy Benzoquinone
• 2,5-Dochloro-3,6-Dohydroxy-P-Benzoquinone
• 2,5-Dochloro-3,6-Dyhydroxybenzoquinone
• 2,5-Dyhydroxy-3,6-2-Benzoquinone
• 3,6-Dichloro-2,5-dihydroxy-1,4-benzoquinone
• 3,6-Dichloro-2,5-dihydroxybenzoquinone
• 4-Dione,2,5-Dichloro-3,6-Dihydroxy-5-Cyclohexadiene-1
• 5-Cyclohexadiene-1,4-Dione,2,5-Dichloro-3,6-Dihydroxy-2
• Chloranilic
• Chloranilic Acid,(2,5-Dichloro-3,6-Dihydroxy-1,4
• Chloranilic Acid Crystalline
• Chlorobenzene Acid
• Dichloro Hydroquinone
• Labotest-Bb Lt00159487
• NSC 6108
• NSC 97383
• P-Benzoquinone, 2,5-Dichloro-3,6-Dihydroxy-
• P-Chloranilicacid
• Quinone, 2,5-dichloro-3,6-dihydroxy-
• Timtec-Bb Sbb008913
• p-Chloranilic acid

Chloranilic Acid

CAS: 87-88-7

Formula: C₆H₂Cl₂O₄

Purity: >98.0%(T)(HPLC)

Color and Shape: Orange to Brown powder to crystal

Molecular weight: 208.98

Ref: 3B-C0077

Chloranilic acid

CAS: 87-88-7

Formula: C₆H₂Cl₂O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 208.9837

Ref: IN-DA003OS1

Chloranilicacid

CAS: 87-88-7

Chloranilicacid

Purity: 95%

Molecular weight: 208.98g/mol

Ref: 54-OR1012638

CHLORANILIC ACID

CAS: 87-88-7

Purity: 97%

Molecular weight: 208.9799957

Ref: 10-F842485

Chloranilic Acid extrapure, 98%

CAS: 87-88-7

Formula: C₆H₂Cl₂O₄

Purity: min.98%

Color and Shape: Orange to Brown, Powder, Clear

Molecular weight: 208.98

Ref: SR-77441

Chloranilic acid

CAS: 87-88-7

Chloranilic acid is a thermally unstable compound that undergoes a number of reactions with the addition of heat. It reacts with nitrogen atoms to form amides, nitriles, and nitro compounds. Chloranilic acid also reacts with polymerases to form stable complexes. The proton at the center of the chloranilic acid molecule is lost when it forms an acid complex. This reaction occurs in aqueous solution as well as in biological systems, where it is used for hydrogen bonding interactions. The stable complexes that are formed by chloranilic acid have been shown to have biological properties such as antimicrobial activity, antiviral activity, and antifungal activity.

Formula: C₆H₂Cl₂O₄

Purity: Min. 95%

Color and Shape: Orange To Red Solid

Molecular weight: 208.98 g/mol

Ref: 3D-FC19926

Chloranilic acid, 98+%

CAS: 87-88-7

Chloranilic acid is used in spectrophotometry. It reacts with metal ions to form stable complexes. It is also used as a reactant in the preparation of dimethylbipyridyl complexes and (nonylbenzimidazolylmethyl)benzene. Further, it is used in charge-transfer reactions with metoprolol tartrate. It is

Formula: C₆H₂Cl₂O₄

Purity: 98+%

Color and Shape: Red to orange or reddish-orange, Powder or crystalline powder

Molecular weight: 208.98

Ref: 02-A10493