7402-70-2

Basic information

• Product Name: N-(2-tert-butylphenyl)acetamide
• CAS NO: 7402-70-2
• Molecular Formula: C₁₂H₁₇NO
• Molecular Weight: 191.2695
• Mol File: 7402-70-2.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 331.1°C at 760 mmHg
• Flash Point: 197.2°C
• Density: 1.01g/cm³
• Vapor Pressure: 0.000159mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: N-(2-tert-butylphenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-tert-butylphenyl)acetamide(7402-70-2)
• EPA Substance Registry System: N-(2-tert-butylphenyl)acetamide(7402-70-2)

Safety Data

• Hazardous Substances Data: 7402-70-2(Hazardous Substances Data)

Usage

General Description

N-(2-tert-butylphenyl)acetamide is a chemical compound that consists of an amide group attached to the acetic acid. It is used as a pharmaceutical intermediate in the synthesis of various drugs. N-(2-tert-butylphenyl)acetamide has potential applications in the field of medicine due to its anti-inflammatory and analgesic properties. It is also used in the development of novel drug candidates for treating various conditions. Additionally, N-(2-tert-butylphenyl)acetamide is known for its role as a corrosion inhibitor in industrial applications. However, it is important to handle this chemical with care and follow proper safety precautions due to its potential hazards.

Upstream product

• 6310-21-0 2-(1,1-dimethylethyl)-benzenamine 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 71-43-2 benzene 
• 1886-57-3 1-tert-butyl-2-nitrobenzene 
• 253185-03-4 tert-butylbenzene 
• 100-46-9 benzylamine 
• 318256-54-1 (RS)-N-(2-tert-butylphenyl)-N-pivaloylacetamide 
• 75-36-5 acetyl chloride 

Downstream Products

• 41085-44-3 2-tert-butyl-6-nitro-aniline 
• 59255-98-0 2-(tert-butyl)-4-nitroaniline 
• 243662-21-7 (RS)-N-(2-tert-butylphenyl)-N-propionylacetamide 
• 342045-15-2 N-(2-tert-butyl-5-nitro-phenyl)-acetamide 
• 1190867-87-8 N-(2-tert-butyl-6-chloro-phenyl)-acetamide 
• 91802-56-1 N-(2-tert-butyl-4-chloro-phenyl)-acetamide 
• 13780-90-0 N-(2-tert-butyl-4-hydroxy-phenyl)-acetamide 
• 1190867-83-4 N-(5-acetyl-2-tert-butyl-phenyl)-acetamide 
• 103392-84-3 2-tert-Butyl-5-nitro-phenylamine 
• 850012-44-1 4-bromo-(2-tert-butyl)aniline 
• 951-14-4 acetic acid-(2-tert-butyl-N-nitroso-anilide) 
• 342045-12-9 acetic acid-(2-tert-butyl-6-nitro-anilide) 
• 1190867-80-1 N-(2-tert-butyl-4-formyl-phenyl)-acetamide 
• 1190867-72-1 N-(2-tert-butyl-4-trimethyl-silanyl-phenyl)-acetamide 

Relevant articles and documents

POLYCYCLIC COMPOUND AND AN ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE POLYCYCLIC COMPOUND OR THE COMPOSITION

Specific polycyclic compounds, a material for an organic electroluminescence device comprising said specific polycyclic compound, an organic electroluminescence device comprising said specific polycyclic compound, an electronic equipment comprising said organic electroluminescence device, a process for preparing said polycyclic compounds, and the use of said polycyclic compounds in an organic electroluminescence. (Formula I) (I)

2,3-DIHYDROQUINAZOLIN COMPOUNDS AS NAV1.8 INHIBITORS

The present invention relates to Nav1.8 Inhibitor 2,3-dihydroquinazolin compounds of Formula (X); wherein Y', X', B', R1', R2', R3', R5', R6', R7', and z1 are as defined herein; or pharmaceutically acceptable salts or tautomer forms thereof, corresponding pharmaceutical compositions or formulations, methods or processes of compound preparation, methods, compounds for use in, uses for and/or combination therapies for treating pain and/or pain-related or associated disease(s), disorder(s) or condition(s), respectively.

Sulfated choline ionic liquid-catalyzed acetamide synthesis by grindstone method

Sulfated choline ionic liquid (SCIL) has been found to be an efficient solid acid IL catalyst for the protection of amine groups with acetic anhydride under solvent-free grindstone conditions. The attractive features of this new catalytic methodology include its sustainability, facile work-up procedure, economic viability, and biodegradability. The SCIL catalyst was characterized using infrared spectroscopy, wide-angle X-ray scattering analysis, and scanning electron microscopy with energy dispersive X-ray spectroscopy. The catalyst could be reused six times without significant loss in activity. Furthermore, no chromatographic separations were needed to obtain the desired products.