23595-42-8

Basic information

• Product Name: 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE
• Synonyms: 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE;2,2',4',5'-TETRACHLOROACETANILIDE;2',4',5'-Trichloro-2-chloroacetanilide;2-chloro-N-(2,4,5-trichlorophenyl)ethanamide;Acetamide, 2-chloro-N-(2,4,5-trichlorophenyl)-;Acetamide, 2-chloro-N-(2,4,5-trichlorophenyl)- (9CI);ACETANILIDE, 2,2',4',5'-TETRACHLORO-;WLN: G1VMR BG DG EG
• CAS NO: 23595-42-8
• Molecular Formula: C₈H₅Cl₄NO
• Molecular Weight: 272.95
• Mol File: 23595-42-8.mol

Chemical Properties

• Melting Point: 137-138.5 °C
• Boiling Point: 405.3°Cat760mmHg
• Flash Point: 198.9°C
• Appearance: /
• Density: 1.607g/cm³
• Vapor Pressure: 8.85E-07mmHg at 25°C
• Refractive Index: 1.625
• PKA: 10.42±0.70(Predicted)
• CAS DataBase Reference: 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE(23595-42-8)
• EPA Substance Registry System: 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE(23595-42-8)

Safety Data

• Hazardous Substances Data: 23595-42-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE is used as a chemical intermediate for the synthesis of pharmaceuticals, contributing to the development of new medications due to its reactive and functional properties.
Used in Pesticide Production:
In the agrochemical sector, 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE serves as a building block in the creation of pesticides, playing a role in enhancing crop protection and yield.
Used in Agrochemicals and Biocides:
2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE is utilized in the production of agrochemicals and biocides, which are essential for controlling pests and diseases in agriculture and other industries, thereby supporting public health and food security.
Used in Chemical Industry:
2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE's versatile reactivity and functional properties make it a valuable component in various chemical processes and the synthesis of different organic compounds, contributing to the advancement of the chemical industry.
Safety Note:
It is crucial to handle 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE with care and adhere to all safety guidelines and regulations to ensure the safe use of 2-CHLORO-N-(2,4,5-TRICHLOROPHENYL)ACETAMIDE in various applications.

InChI:InChI=1/C8H5Cl4NO/c9-3-8(14)13-7-2-5(11)4(10)1-6(7)12/h1-2H,3H2,(H,13,14)

Upstream product

• 79-04-9 chloroacetyl chloride 
• 636-30-6 2,4,5-trichloroaniline 

Downstream Products

• 97457-63-1 3-Hydroxy-benzo[b]thiophene-2-carboxylic acid (2,4,5-trichloro-phenyl)-amide 
• 1018074-66-2 C₁₆H₉Cl₅FN₅OS 

Relevant articles and documents

Synthesis, Molecular Docking and Biological Evaluation of 2-Aryloxy-N-Phenylacetamide and N′-(2-Aryloxyoxyacetyl) Benzohydrazide Derivatives as Potential Antibacterial Agents

A new class of 2-aryloxy-N-phenylacetamide and N′-(2-aryloxyoxyacetyl) benzohydrazide derivatives with different active moieties were synthesized and screened for their antibacterial activity. Structural characterization of synthesized compounds was perfo

Synthesis and biological evaluation of N-(substituted phenyl)-2-(5H-[1,2,4]triazino[5,6-b]indol-3-ylsulfanyl)acetamides as antimicrobial, antidepressant, and anticonvulsant agents

A new series of N-Aryl-2-(5H-[1,2,4]triazino[5,6-b]indol-3-ylsulfanyl)acetamides were synthesized by condensation of tricyclic compound 2,5-dihydro-3H-[1,2,4]triazino[5,6-b]indole-3-thione with chloro N-phenylacetamides. The tricyclic compound was obtaine

Activities of 2-carboxanilido 3-hydroxybenzo[b]thiophens against molluscs Biomphalaria

The title compounds are shown to be nearly as active against molluscs as Niclosamide when they are either dihalogenated or monohalogenated and mononitrated on the benzene ring.