17892-26-1

Basic information

• Product Name: 3,5-Dichloro-2-Hydroxy Benzamide
• Synonyms: 3,5-Dichloro-2-Hydroxy Benzamide;Benzamide, 3,5-dichloro-2-hydroxy-
• CAS NO: 17892-26-1
• Molecular Formula: C₇H₅Cl₂NO₂
• Molecular Weight: 206.0261
• Mol File: 17892-26-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 267.3 °C at 760 mmHg
• Flash Point: 115.5 °C
• Appearance: /
• Density: 1.579 g/cm³
• Vapor Pressure: 0.00498mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: 3,5-Dichloro-2-Hydroxy Benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dichloro-2-Hydroxy Benzamide(17892-26-1)
• EPA Substance Registry System: 3,5-Dichloro-2-Hydroxy Benzamide(17892-26-1)

Safety Data

• Hazardous Substances Data: 17892-26-1(Hazardous Substances Data)

Usage

General Description

3,5-Dichloro-2-Hydroxy Benzamide is a chemical compound with the molecular formula C7H5Cl2NO2. It is a derivative of benzamide and contains two chlorine atoms and a hydroxy group attached to a benzene ring. 3,5-Dichloro-2-Hydroxy Benzamide is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs. It has also been studied for its potential anti-cancer properties and its ability to inhibit certain enzymes. Additionally, it is used in the manufacturing of pigments and dyes. The chemical properties and structure of 3,5-Dichloro-2-Hydroxy Benzamide make it a valuable tool for various applications in the fields of medicine, chemistry, and industry.

InChI:InChI=1/C7H5Cl2NO2/c8-3-1-4(7(10)12)6(11)5(9)2-3/h1-2,11H,(H2,10,12)

Upstream product

• 65-45-2 salicylamide 
• 320-72-9 3,5-dichlorosalicylic acid 
• 39614-80-7 3,5-dichloro-2-hydroxy-benzoyl chloride 

Downstream Products

• 17892-00-1 3,5-dichloro-2-hydroxy-N-morpholin-4-ylmethyl-benzamide 
• 724706-53-0 3,5-dichloro-2-hydroxy-benzoic acid-(2,2,2-trichloro-1-hydroxy-ethylamide) 

Relevant articles and documents

Continuous-Flow Hofmann Rearrangement Using Trichloroisocyanuric Acid for the Preparation of 2-Benzoxazolinone

A continuous-flow preparation of 2-benzoxazolinone via the Hofmann rearrangement of salicylamide has been implemented employing trichloroisocyanuric acid as the stable and atom-economic chlorinating agent. The system was optimized to avoid solid accumulation and allow the preparation of hundreds of grams of the pure desired material over a working day. Furthermore, a trichloroisocyanuric acid (TCCA)-based chlorination of 2-benzoxazolone to the corresponding 5-chloro derivative was also carried out under batch conditions.

Certain benzoxazoles and the use thereof as metal extractants

Benzoxazoles having the structure STR1 where R is hydrogen or an alkyl group having from 1 to 20 carbon atoms, R' is hydrogen, chlorine or an alkyl group containing from 1 to 20 carbon atoms, X is H or Chlorine and the total number of carbon atoms in R an