CAS 86-47-5

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

Description:

7-Chloro-4-hydroxyquinoline-3-carboxylic acid, with the CAS number 86-47-5, is a chemical compound that belongs to the class of quinoline derivatives. It is characterized by the presence of a chloro group at the 7-position, a hydroxy group at the 4-position, and a carboxylic acid functional group at the 3-position of the quinoline ring. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals, particularly as an antibacterial agent. Its structure contributes to its biological activity, allowing it to interact with various biological targets. The presence of the carboxylic acid group enhances its solubility in polar solvents, while the chloro and hydroxy groups can influence its reactivity and binding properties. Additionally, 7-Chloro-4-hydroxyquinoline-3-carboxylic acid may exhibit fluorescence, making it useful in certain analytical applications. As with many chemical substances, proper handling and safety precautions are essential due to its potential biological effects.

Formula: C₁₀H₆ClNO₃

InChI: InChI=1S/C10H6ClNO3/c11-5-1-2-6-8(3-5)12-4-7(9(6)13)10(14)15/h1-4H,(H,12,13)(H,14,15)

InChI key: InChIKey=SACLIBNEKWTDEG-UHFFFAOYSA-N

SMILES: OC=1C2=C(N=CC1C(O)=O)C=C(Cl)C=C2

Synonyms:

• 3-Carboxy-4-hydroxy-7-chloroquinoline
• 3-Quinolinecarboxylic acid, 7-chloro-4-hydroxy-
• 4-Hydroxy-7-chloro-3-quinolinecarboxylic acid
• 4-Hydroxy-7-chloroquinoline-3-carboxylicacid
• 4-Hydroxy-7-chloroquinoline-3-caroboxylic acid
• 7-Chloro-4-Oxo-1,4-Dihydroquinoline-3-Carboxylic Acid
• 7-Chloro-4-hydroxy-3-quinolinecarboxylic acid
• Ai3-23857
• Brn 0171561
• NSC 56803
• Nsc 27801
• Quinoline, 3-carboxy-4-hydroxy-7-chloro-
• Usaf Kf-16
• 5-22-05-00286 (Beilstein Handbook Reference)

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

CAS: 86-47-5

Formula: C₁₀H₆ClNO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 223.6125

Ref: IN-DA003NEI

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

CAS: 86-47-5

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

Purity: 99%

Molecular weight: 223.61254g/mol

Ref: 54-OR183478

Hydroxychloroquine Impurity 13

CAS: 86-47-5

Formula: C₁₀H₆ClNO₃

Molecular weight: 223.61

Ref: 4Z-H-0632

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

CAS: 86-47-5

7-Chloro-4-hydroxyquinoline-3-carboxylic acid is a chemical compound that has antioxidative activity and is used in the production of various organic substances. It is synthesized by reacting ammonium nitrate with a hydroxy group, an organic solvent, and phenoxy. The resulting product can be heated to form 7-chloro-4-hydroxyquinoline, which undergoes a series of reactions to produce 7-chloro-4-(2,2,2,-trichloroethoxy)quinoline. This reaction system produces a quinoline derivative that has been shown to be expressed at high levels in phosphatidylcholine (PC) and alpha-tocopherol (a vitamin E derivative). The final product is then purified by triethyl orthoformate (TEO), which removes the sulfoxide group.

Formula: C₁₀H₆ClNO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 223.61 g/mol

Ref: 3D-FC44132

7-Chloro-4-hydroxyquinoline-3-carboxylic acid

CAS: 86-47-5

Formula: C₁₀H₆ClNO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 223.61

Ref: 10-F211179

7-Chloro-4-hydroxyquinoline-3-carboxylic Acid

Controlled Product

CAS: 86-47-5

Applications 7-chloro-4-hydroxyquinoline-3-carboxylic acid (cas# 86-47-5) is a useful research chemical.

Formula: C₁₀H₆ClNO₃

Color and Shape: Neat

Molecular weight: 223.61

Ref: TR-C382335

Hydroxychloroquine Impurity 9

CAS: 86-47-5

Formula: C₁₀H₆ClNO₃

Molecular weight: 223.61

Ref: ST-EA-CP-H4036