400750-84-7

Basic information

• Product Name: 2-(5-METHYL-2-FURYL)ANILINE, 95
• Synonyms: 2-(5-METHYL-2-FURYL)ANILINE, 95;2-(5-Methylfuran-2-yl)aniline
• CAS NO: 400750-84-7
• Molecular Formula: C₁₁H₁₁NO
• Molecular Weight: 173.214
• Mol File: 400750-84-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(5-METHYL-2-FURYL)ANILINE, 95(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(5-METHYL-2-FURYL)ANILINE, 95(400750-84-7)
• EPA Substance Registry System: 2-(5-METHYL-2-FURYL)ANILINE, 95(400750-84-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 400750-84-7(Hazardous Substances Data)

Usage

General Description

2-(5-Methyl-2-furyl)aniline, 95 is a chemical compound with the molecular formula C11H11NO. It is a pale yellow to brownish solid with a melting point of around 58-60°C. 2-(5-METHYL-2-FURYL)ANILINE, 95 is commonly used as an intermediate in the synthesis of various pharmaceuticals, dyes, and agrochemicals. It is also used in the production of rubber chemicals and as a dye intermediate. Additionally, 2-(5-Methyl-2-furyl)aniline, 95 is known for its potential health hazards and should be handled with care, as it may cause skin and eye irritation, and is harmful if swallowed or inhaled.

Upstream product

• 20000-96-8 5-(2-nitrophenyl)-2-furaldehyde 
• 62306-79-0 5-methylfuran-2-boronic acid 
• 615-36-1 2-bromoaniline 
• 88-74-4 2-nitro-aniline 
• 98-01-1 furfural 
• 1045704-61-7 2-methyl-5-(2-nitrophenyl)-furan 

Downstream Products

• 239-09-8 11H-indolo[3,2-c]quinoline 
• 1353023-91-2 C₁₃H₁₄N₂O₂ 
• 1353023-85-4 2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-N-[2-(5-methyl-2-furyl)phenyl]acetamide 
• 1219474-62-0 (3E)-4-[2-(2-nitrophenyl)-1H-indol-3-yl]but-3-en-2-one 
• 1219474-50-6 (3E)-4-[2-(3,4-dimethoxyphenyl)-1H-indol-3-yl]but-3-en-2-one 
• 1219474-56-2 (3E)-4-[2-(4-nitrophenyl)-1H-indol-3-yl]but-3-en-2-one 
• 1219474-59-5 (3E)-4-[2-(3-nitrophenyl)-1H-indol-3-yl]but-3-en-2-one 
• 1219474-53-9 (3E)-4-[2-(4-fluorophenyl)-1H-indol-3-yl]but-3-en-2-one 
• 1219474-95-9 (3E)-4-{2-[5-(2,4,6-trichlorophenyl)-2-furyl]-1H-indol-3-yl}but-3-en-2-one 
• 1219474-98-2 (3E)-4-{2-[5-(4-methyl-2-nitrophenyl)-2-furyl]-1H-indol-3-yl}but-3-en-2-one 
• 1045704-70-8 C₁₂H₉NOS 

Relevant articles and documents

Gold-Catalyzed Cascade Reactions of 4 H-Furo[3,2-b]indoles with Allenamides: Synthesis of Indolin-3-one Derivatives

Merging the ability of cationic gold(I) catalysts to activate unsaturated π-systems with the electrophiles-driven ring-opening reactions of furans, we describe a new approach to synthesize 2-spiroindolin-3-ones from 4H-furo[3,2-b]indoles. The reaction occ

A new simple route to the thieno[2,3-b]indole ring system

A simple and effective method has been elaborated for the synthesis of thieno[2,3-b]indole ring system. It is based on the electrophilic recyclization of 2-alkyl-5-(2-isothiocyanoaryl)furans in the presence of anhydrous AlCl 3. Georg Thieme Ver

2-(anilinomethyl)imidazolines as alpha1A adrenergic receptor agonists: 2'-heteroaryl and 2'-oxime ether series.

A series of 2'-heteroaryl and 2'-oxime anilinomethylimidazolines was prepared and evaluated in in vitro functional assays for cloned human alpha1A, alpha1B, and alpha1D receptor subtypes. Potent and selective alpha1A agonists have been identified in these series.