5980-26-7

Basic information

• Product Name: 2,3-DICHLOROBENZAMIDE
• Synonyms: 2,3-DICHLOROBENZAMIDE;2,5-DICHLOROBENZAMIDE
• CAS NO: 5980-26-7
• Molecular Formula: C₇H₅Cl₂NO
• Molecular Weight: 190.03
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Anilines, Amides & Amines;Chlorine Compounds
• Mol File: 5980-26-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 170-172°C
• Boiling Point: 262.8 °C at 760 mmHg
• Flash Point: 112.7 °C
• Appearance: /
• Density: 1.439 g/cm³
• Vapor Pressure: 0.0107mmHg at 25°C
• Refractive Index: 1.596
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.77±0.50(Predicted)
• CAS DataBase Reference: 2,3-DICHLOROBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DICHLOROBENZAMIDE(5980-26-7)
• EPA Substance Registry System: 2,3-DICHLOROBENZAMIDE(5980-26-7)

Safety Data

• Hazard Codes: Xi:
• Statements: R36/37/38:
• Safety Statements: 24/25
• Hazardous Substances Data: 5980-26-7(Hazardous Substances Data)

Usage

General Description

2,3-Dichlorobenzamide is a chemical compound with the molecular formula C7H5Cl2NO. It is a white solid at room temperature and is soluble in organic solvents. 2,3-Dichlorobenzamide is used as an intermediate in the synthesis of other organic compounds. It can also be used as a pesticide and herbicide. It is considered to be relatively stable under normal conditions, but it may release toxic fumes when heated to decomposition. 2,3-Dichlorobenzamide should be handled with care and proper protective equipment should be worn when working with this chemical.

InChI:InChI=1/C7H5Cl2NO/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H2,10,11)

Upstream product

• 50-79-3 2,5-dichlorobenzoic acid 
• 106-46-7 para-dichlorobenzene 
• 127099-85-8 N-Cyanoguanidine 
• 2905-61-5 2,5-dichlorobenzoyl chloride 
• 618-48-4 3-chlorobenzamide 

Downstream Products

• 104326-58-1 ethyl 2,5-dichlorobenzimidate 
• 1143020-21-6 2,5-dichloro-N-[(6-methylsulfonylbenzothiazol-2-yl)carbamoyl]benzamide 
• 69622-81-7 2,5-dichlorothiobenzamide 

Relevant articles and documents

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Design, synthesis and fungicidal activity of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamide

To find a new lead compound with high biological activity, a series of N-substituted benzoyl-1,2,3,4-tetrahydroquinolyl-1-carboxamide were designed using linking active substructures method. The target compounds were synthesized from substituted benzoic acid by four steps and their structures were confirmed by 1H NMR, IR spectrum and elemental analysis. The in vitro bioassay results indicated that some target compounds exhibited excellent fungicidal activities, and the position of the substituents played an important role in fungicidal activities. Especially, compound 5n, exhibited better fungicidal activities than the commercial fungicide flutolanil against two tested fungi Valsa Mali and Sclerotinia sclerotiorum, with EC50 values of 3.44 and 2.63 mg/L, respectively. And it also displayed good in vivo fungicidal activity against S. sclerotiorum with the EC50 value of 29.52 mg/L.