23410-20-0

Basic information

• Product Name: 2,5-dimethyl-4-aminoacetanilide
• CAS NO: 23410-20-0
• Molecular Weight: 178.234
• Mol File: 23410-20-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,5-dimethyl-4-aminoacetanilide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-dimethyl-4-aminoacetanilide(23410-20-0)
• EPA Substance Registry System: 2,5-dimethyl-4-aminoacetanilide(23410-20-0)

Safety Data

• Hazardous Substances Data: 23410-20-0(Hazardous Substances Data)

Usage

General Description

2,5-dimethyl-4-aminoacetanilide is a chemical compound with the molecular formula C10H14N2O. It is a derivative of acetanilide, which is commonly used as an analgesic and fever-reducing medication. The chemical is a white to slightly pink powder with a melting point of 94-96°C and is sparingly soluble in water. It is used as an intermediate in the synthesis of various pharmaceuticals and dyes, and it also has applications in the field of organic chemistry. The compound is an amide derivative with a dimethyl substitution at the 2 and 5 positions on the phenyl ring, as well as an amino group at the 4 position.

Upstream product

• 3460-29-5 4-nitro-2,5-xylidine 
• 95-78-3 2,5-Dimethylaniline 
• 6954-69-4 N-(2,5-dimethyl-4-nitrophenyl)acetamide 
• 7803-57-8 hydrazine hydrate 
• 2050-44-4 N-(2,5-dimethylphenyl)acetamide 

Downstream Products

• 106423-99-8 2,2′,5,5′-tetramethyl-4,4′-azodiacetanilide 

Relevant articles and documents

Variable noninnocence of substituted azobis(phenylcyanamido)diruthenium complexes

The synthetic chemistry of substituted 4,4′-azobis(phenylcyanamide) ligands was investigated, and the complexes [{Ru(tpy)(bpy)}2( μ-L)][PF6]2, where L = 2,2′:5,5′-tetramethyl-4,4′-azobis(phenylcyanamido) (Me4adpc2-), 2,2′-dimethyl-4,4′-azobis(phenylcyanamido) (Me2adpc2-), unsubstituted (adpc2-), 3,3′-dichloro-4,4′-azobis(phenylcyanamido) (Cl2adpc2-), and 2,2′:5,5′-tetrachloro-4,4′-azobis(phenylcyanamido) (Cl4adpc2-), were prepared and characterized by cyclic voltammetry and vis-near-IR (NIR) and IR spectroelectrochemistry. The room temperature electron paramagnetic resonance spectrum of [{Ru(tpy)(bpy)}2( μ-Me4adpc)]3+ showed an organic radical signal and is consistent with an oxidation-state description [RuII, Me4adpc?-, RuII]3+, while that of [{Ru(tpy)(bpy)}2( μ-Cl2adpc)]3+ at 10 K showed a low-symmetry RuIII signal, which is consistent with the description [RuIII, Cl2adpc2-, RuII]3+. IR spectroelectrochemistry data suggest that [{Ru(tpy)(bpy)}2( μ-adpc)]3+ is delocalized and [{Ru(tpy)(bpy)}2( μ-Cl2adpc)]3+ and [{Ru(tpy)(bpy)}2( μ-Cl4adpc)]3+ are valence-trapped mixed-valence systems. A NIR absorption band that is unique to all [{Ru(tpy)(bpy)}2( μ-L)]3+ complexes is observed; however, its energy and intensity vary depending on the nature of the bridging ligand and, hence, the complexes oxidation-state description.