5959-39-7

Usage

Chemical compound

2-amino-4,6-dichlorophenol hydrochloride

Physical appearance

White to off-white crystalline powder

Primary use

Manufacturing of pharmaceuticals, especially antiseptic and antibacterial agents

Properties

Antifungal, antibacterial

Application

Topical treatments for skin infections

Other uses

pH indicator, production of dyes

Potential hazards

Harmful if ingested or inhaled, may cause irritation to the skin and eyes

Precautions

Proper handling and storage required

Upstream product

• 609-89-2 2,4-dichloro-6-nitrophenol 

Downstream Products

• 63969-35-7 2,4-dichloro-6-diazocyclohexa-2,4-dien-1-one 
• 944356-40-5 2-bromo-N-(3,5-dichloro-2-hydroxyphenyl)-3-methylbutyramide 
• 98192-46-2 Acetic acid 5,7-dichloro-2-phenyl-2,3-dihydro-benzofuran-2-yl ester 
• 54932-85-3 5,7-dichloro-2-methylbenzofuran 

Relevant academic research and scientific papers

Carboxylic Acid Compounds and Use Thereof

Provision of a superior URAT1 activity inhibitor effective for the treatment and the like of a pathology involving uric acid, such as hyperuricemia, gouty tophus, acute gouty arthritis, chronic gouty arthritis, gouty kidney, urinary lithiasis, renal dysfunction, coronary heart disease, ischemic cardiac diseases and the like. A URAT1 activity inhibitor containing a compound represented by the following formula [1] or a pharmaceutically acceptable salt thereof, or a solvate thereof as an active ingredient: [image] wherein each symbol is as defined in the specification.

QUINONE DIAZIDE CYCLIZATIONS - A DIRECT ROUTE TO DIHYDROBENZOFURANS

The reaction of ortho-quinone diazides with electron-rich alkenes produces 2,3-dihydrobenzofurans.The ortho-quinone diazides are formed the ortho-nitrophenols by reduction and diazotization.The reaction of an ortho-quinone diazide with 2,3-dihydrofuran produces a furo-benzofuran ring system.