7160-08-9

Basic information

• Product Name: N-(4-bromophenyl)-2-methylpropanamide
• Synonyms: N-(4-bromophenyl)-2-methylpropanamide;UKRORGSYN-BB BBV-077135;N-(4-bromophenyl)-2-methylpropanamide(SALTDATA: FREE);PropanaMide, N-(4-broMophenyl)-2-Methyl-
• CAS NO: 7160-08-9
• Molecular Formula: C₁₀H₁₂BrNO
• Molecular Weight: 242.11
• Mol File: 7160-08-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 364°C at 760 mmHg
• Flash Point: 173.9°C
• Appearance: /
• Density: 1.406g/cm³
• Vapor Pressure: 1.73E-05mmHg at 25°C
• Refractive Index: 1.582
• CAS DataBase Reference: N-(4-bromophenyl)-2-methylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-bromophenyl)-2-methylpropanamide(7160-08-9)
• EPA Substance Registry System: N-(4-bromophenyl)-2-methylpropanamide(7160-08-9)

Safety Data

• Hazardous Substances Data: 7160-08-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H12BrNO/c1-7(2)10(13)12-9-5-3-8(11)4-6-9/h3-7H,1-2H3,(H,12,13)

Upstream product

• 4406-41-1 N-phenylisobutyramide 
• 79-31-2 isobutyric Acid 
• 79-30-1 isobutyryl chloride 
• 78-82-0 Isobutyronitrile 
• 139139-81-4 bis(4-bromophenyl)iodonium triflate 

Downstream Products

• 1401771-41-2 N-(4-bromophenyl)isobutyrthioamide 
• 1444024-22-9 (E)-N-(4-(1',2'-bis(4'',4'''-(benzyloxy)phenyl)but-1'-enyl)phenyl)isobutyramide 
• 1444024-37-6 (Z)-N-(4-(1',2'-bis(4'',4'''-(benzyloxy) phenyl) but-1'-enyl)phenyl)isobutyramide 
• 1444024-52-5 (E)-N-(4-(1',2'-bis(4'',4'''-hydroxyphenyl)-but-1'-enyl)phenyl)hexanamide 
• 1444024-67-2 (Z)-N-(4-(1',2'-bis(4'',4'''-hydroxyphenyl)-but-1'-enyl) phenyl)isobutyramide 
• 1444023-98-6 N-(4-(4'-(benzyloxy)benzoyl)phenyl)isobutyramide 
• 1444023-83-9 N-(4-((4'-(benzyloxy)phenyl)(hydroxy)-methyl)phenyl)isobutyramide 
• 6876-49-9 N-(4-methylphenyl)-2,2-dimethylacetamide 
• 134811-06-6 methyl 2-(4-isobutyramidophenyl)propanoate 

Relevant articles and documents

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Preparation method of N-aryl amide compound

The invention discloses a preparation method of an N-aryl amide compound, which comprises the following steps: (1) putting diaryliodonium salt and Cu(OAc)2 into a Schlenk tube provided with a magneticstirring rod; (2) sequentially adding DCE, H2O and nitrile by using an injector, sealing the Schlenk tube, and stirring for reaction at 80 DEG C; (3) cooling the obtained solution to room temperature, and performing extraction with EtOAc; and combining organic layers, performing washing with saline water, and performing drying with anhydrous Na2SO4; and (4) removing volatile matters in vacuum, and purifying residues through column chromatography to obtain the N-aryl amide compound. Through a large number of experiments, a substrate with a simple structure is screened, the reaction conditionsare mild, the yield is high, the pollution is small, and the application prospect is wide.

Organometallic Complex, Light-Emitting Element, Display Device, Electronic Device, and Lighting Device

An organometallic complex which can emit phosphorescence is provided. The organometallic complex, which is a novel substance, is represented by General Formula (G1) or General Formula (G2). In General Formula (G1), R1 to R10 each represent an alkyl group having 1 to 4 carbon atoms. M represents a Group 9 element or a Group 10 element. When M is a Group 9 element, n is 3, and when M is a Group 10 element, n is 2. In General Formula (G2), R11 to R20 each represent an alkyl group having 1 to 4 carbon atoms. M represents a Group 9 element or a Group 10 element. When M is a Group 9 element, n is 3, and when M is a Group 10 element, n is 2.