2050-44-4

Basic information

• Product Name: 2',4'-DIMETHYLACETANILIDE
• Synonyms: 2',4'-ACETOXYLIDIDE;2',4'-DIMETHYLACETANILIDE;2,4-DIMETHYLACETANILIDE;N-ACETYL-2',4'-XYLIDINE;N-ACETYL-2,4-XYLIDINE;2,5-dimethylacetanilide;2’,5’-acetoxylidide;2’,5’-dimethyl-acetanilid
• CAS NO: 2050-44-4
• Molecular Formula: C₁₀H₁₃NO
• Molecular Weight: 163.22
• Mol File: 2050-44-4.mol
• Article Data: 28

Chemical Properties

• Melting Point: 129-132 °C(lit.)
• Boiling Point: 292.8°Cat760mmHg
• Flash Point: 169.7°C
• Appearance: /
• Density: 1.052g/cm³
• Vapor Pressure: 0.00179mmHg at 25°C
• Refractive Index: 1.56
• CAS DataBase Reference: 2',4'-DIMETHYLACETANILIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2',4'-DIMETHYLACETANILIDE(2050-44-4)
• EPA Substance Registry System: 2',4'-DIMETHYLACETANILIDE(2050-44-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-36/37
• WGK Germany: 3
• RTECS: AN7420000
• Hazardous Substances Data: 2050-44-4(Hazardous Substances Data)

Usage

General Description

2',4'-DIMETHYLACETANILIDE is a chemical compound with the molecular formula C10H13NO. It is an organic compound and an amide derivative of acetanilide. The compound consists of a benzene ring substituted with two methyl groups at the 2' and 4' positions, as well as an acetamide functional group. 2',4'-DIMETHYLACETANILIDE is commonly used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds. It is also utilized in the production of dyes and pigments. Additionally, it has potential applications in the field of organic chemistry and as a reagent in research and laboratory settings.

InChI:InChI=1/C10H13NO/c1-7-4-5-8(2)10(6-7)11-9(3)12/h4-6H,1-3H3,(H,11,12)

Upstream product

• 15329-10-9 3,6-dimethylcyclohex-2-enone 
• 75-36-5 acetyl chloride 
• 537-92-8 3-Methylacetanilide 
• 74-88-4 methyl iodide 
• 95-78-3 2,5-Dimethylaniline 
• 106-42-3 para-xylene 
• 75-05-8 acetonitrile 
• 17075-25-1 1,4-dimethyl-2-nitrosobenzene 
• 431-03-8 dimethylglyoxal 
• 123-54-6 acetylacetone 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 5692-34-2 2,5-dimethylbenzamide 
• 64-19-7 acetic acid 
• 108-24-7 acetic anhydride 

Downstream Products

• 194735-89-2 acetic acid-(2,4-dichloro-3,6-dimethyl-anilide) 
• 873979-22-7 acetic acid-(2,4,5-trichloro-3,6-dimethyl-anilide) 
• 80539-09-9 4-amino-2,5-dimethylacetophenone 
• 65266-52-6 N-acetyl-4-amino-2,5-dimethylacetophenone 
• 51786-47-1 N-phenyl-2,5-dimethylacetanilide 
• 6954-69-4 N-(2,5-dimethyl-4-nitrophenyl)acetamide 
• 27897-08-1 4-Amino-2,5-dimethylbenzenesulfonic Acid 
• 227467-72-3 4'-(2-bromoacetyl)-2',5'-dimethylacetanilide 
• 117780-48-0 N-(2,5-Dimethyl-phenyl)-N-((E)-octa-2,7-dienyl)-acetamide 
• 13711-31-4 N-(4-bromo-2,5-dimethyl-phenyl)acetamide 
• 13632-08-1 4-acetylamino-2,5-dimethyl-benzenesulfonyl chloride 
• 99185-32-7 2-acetamidoterephthalic acid 
• 15540-85-9 2,5-dimethyl-6-nitroaniline 
• 3460-29-5 4-nitro-2,5-xylidine 

Relevant articles and documents

NOVEL AGROCHEMICAL COMPOSITION COMPRISING 4-SUBSTITUTED PHENYLAMIDINE COMPOUNDS

The present invention discloses a novel agrochemical composition comprising (1) at lease one compound of formula (I) wherein, R1, R2, R3, R4, R5, R6, R7 and m are as defined in t

Catalyst-free generation of acyl radicals induced by visible light in water to construct C-N bonds

We describe herein a catalyst-free and redox-neutral photochemical strategy for the direct generation of acyl radicals from α-diketones, and its selective conversion of nitrosoarenes to hydroxyamides or amides with AcOH or NaCl as an additive. The reaction was carried out under mild conditions in water with purple LEDs as the light source. A broad scope of substrates was demonstrated. Mechanistic experiments indicate that α-diketones cleave to give acyl radicals, with hydroxyamides being further reduced to amides.

Acylation of Phenols, Alcohols, Thiols, Amines and Aldehydes Using Sulfonic Acid Functionalized Hyper-Cross-Linked Poly(2-naphthol) as a Solid Acid Catalyst

Abstract: The hyper-cross-linked porous poly(2-naphthol) fabricated by the Friedel–Crafts alkylation of 2-naphthol has been functionalized with sulfonic acid to obtain a solid acid catalyst. The catalyst is applied for the protection of phenol, alcohols, thiols, amines and aldehydes with acetic anhydride at room temperature. The catalytic protection using the new solid acid is featured by achieving high yield at neat condition, needing no aqueous work-up and/or chromatographic separation, and showing excellent recycling efficiency, suggesting the potential of this sulfonated porous polymers as a new protection protocol in a wide range of sustainable chemical reactions. Graphical Abstract: [Figure not available: see fulltext.].