38411-17-5

Basic information

• Product Name: N-(2,5-dichloro-4-nitrophenyl)acetamide
• Synonyms: N-(2,5-dichloro-4-nitrophenyl)acetamide;2,5 DICHLORO 4-NITRO ACETINILIDE 99 % BY G.C.
• CAS NO: 38411-17-5
• Molecular Formula: C₈H₆Cl₂N₂O₃
• Molecular Weight: 249.05084
• EINECS: 253-917-5
• Mol File: 38411-17-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 424.6°Cat760mmHg
• Flash Point: 210.6°C
• Appearance: /
• Density: 1.573g/cm³
• CAS DataBase Reference: N-(2,5-dichloro-4-nitrophenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,5-dichloro-4-nitrophenyl)acetamide(38411-17-5)
• EPA Substance Registry System: N-(2,5-dichloro-4-nitrophenyl)acetamide(38411-17-5)

Safety Data

• Hazardous Substances Data: 38411-17-5(Hazardous Substances Data)

Usage

General Description

N-(2,5-dichloro-4-nitrophenyl)acetamide is a chemical compound that belongs to the class of acetamides. It is derived from acetamide and contains 2,5-dichloro-4-nitrophenyl as a substituent. N-(2,5-dichloro-4-nitrophenyl)acetamide is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential antibacterial and antifungal properties. The chemical structure of N-(2,5-dichloro-4-nitrophenyl)acetamide makes it suitable for various applications in the fields of medicine and agriculture, showcasing its potential as a versatile and useful chemical compound.

Upstream product

• 2621-62-7 2,5-dichloroacetanilide 
• 7697-37-2 nitric acid 
• 6627-34-5 2,5-dichloro-4-nitroaniline 
• 75-36-5 acetyl chloride 

Downstream Products

• 6627-34-5 2,5-dichloro-4-nitroaniline 
• 6392-96-7 2,5-dichloro-4-aminoacetanilide 
• 476660-79-4 dimethyl [5-(acetylamino)-4-chloro-2-nitrophenyl]malonate 
• 17801-99-9 1,4-dichloro-2-methoxy-5-nitrobenzene 
• 119-21-1 1-chloro-2,4-dimethoxy-5-nitrobenzene 
• 97-50-7 5-chloro-2,4-dimethoxyaniline 
• 17488-25-4 1,4-dichloro-2,5-dinitrobenzene 
• 62406-69-3 2,3,6-trichloro-4-nitro-aniline 
• 879-39-0 2,3,4,5-tetrachloronitrobenzene 
• 781-15-7 1,2,3,4-tetrachloro-5,6-dinitrobenzene 

Relevant articles and documents

Construction of interconnected acidity functions based on ortho substituted anilines and N-methylanilines as indicators

The log I values of 15 mainly ortho substituted derivatives of aniline and N-methylaniline have been measured spectrophotometrically in sulfuric, perchloric, and methanesulfonic acids. A new algorithm has been suggested for construction of acidity functions enabling simultaneous and independent construction of acidity functions in various media under the condition of equal values of pKa of the same indicators in the given media. The so-called interconnected acidity functions have been constructed with using this algorithm and the log I values measured in the above media, and the pKa values have been calculated. The resulting acidity functions and pKa values agree well with the corresponding literature data.