58217-60-0

Basic information

• Product Name: CHEMBRDG-BB 5245988
• Synonyms: CHEMBRDG-BB 5245988;5-BROMO-N-PHENYL-2-FURAMIDE;5-bromo-N-phenyl-2-furamide(SALTDATA: FREE)
• CAS NO: 58217-60-0
• Molecular Formula: C₁₁H₈BrNO₂
• Molecular Weight: 266.09
• Mol File: 58217-60-0.mol

Chemical Properties

• Boiling Point: 272.1°C at 760 mmHg
• Flash Point: 118.3°C
• Appearance: /
• Density: 1.59g/cm³
• Vapor Pressure: 0.00621mmHg at 25°C
• Refractive Index: 1.647
• CAS DataBase Reference: CHEMBRDG-BB 5245988(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 5245988(58217-60-0)
• EPA Substance Registry System: CHEMBRDG-BB 5245988(58217-60-0)

Safety Data

• Hazardous Substances Data: 58217-60-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H8BrNO2/c12-10-7-6-9(15-10)11(14)13-8-4-2-1-3-5-8/h1-7H,(H,13,14)

Upstream product

• 26726-16-9 5-bromofuran-2-carbonyl chloride 
• 62-53-3 aniline 
• 585-70-6 5-bromo-furan-2-carboxylic acid 

Downstream Products

• 117845-33-7 5-Pyrrolidin-1-yl-furan-2-carboxylic acid phenylamide 
• 117845-32-6 5-Morpholin-4-yl-furan-2-carboxylic acid phenylamide 
• 1107619-37-3 5-{4-[3-(6-Methylpyridin-2-yl)prop-2-ynylidene]piperidin-1-yl}-N-phenyl-2-furamide 

Relevant articles and documents

High-load, soluble oligomeric carbodiimide: Synthesis and application in coupling reactions

A facile preparation of a high-load, soluble oligomeric alkyl cyclohexylcarbodiimide (OACC) reagent via ROM polymerization from commercially available starting materials is described. This reagent is exploited as a coupling reagent for esterification, amidation, and dehydration of carboxylic acids (aliphatic and aromatic) with an assortment of alcohols (aliphatic primary, secondary, and benzylic), thiols, phenols, and amines (aliphatic primary, secondary, benzylic, and aromatic/anilines), respectively. Following the coupling event, precipitation with an appropriate solvent (Et2O, MeOH, or EtOAc), followed by filtration through a SPE provides the products in good to excellent yield and purity.

Antimuscarinic 3-(2-Furanyl)quinuclidin-2-ene derivatives: Synthesis and structure-activity relationships

A series of 25 derivatives of the muscarinic antagonist 3-(2- furanyl)quinuclidin-2-ene (4) was synthesized and evaluated for muscarinic and antimuscarinic properties. Substitution at all three positions of the furan ring has been investigated. The affini

Chemistry of furans: Part VIII - Synthesis of 5-dialkylamino-2-furanamides and furanopeptides

The synthesis of 5-dialkylamino-furanamides by the nucleophilic displacement of bromine on 5-bromo-2-furanamides with pyrrolidine, piperidine and morpholine is described.Several other primary and secondary amines as well as nucleophiles such as sodio amid

Chemistry of Furans: Part VI - Synthesis of 5-Amino-2-furanamides

5-Amino-2-furanamides (II) have been synthesised by the nucleophilic displacement of bromine in 5-bromo-2-furanamides by piperidine, pyrrolidine and morpholine.