5927-94-6

Basic information

• Product Name: N-[2-(2,4-dichlorophenoxy)ethyl]-1-benzofuran-2-carboxamide
• CAS NO: 5927-94-6
• Molecular Formula: C₁₀H₁₁BrO
• Molecular Weight: 350.196
• Mol File: 5927-94-6.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 562.8°C at 760 mmHg
• Flash Point: 294.2°C
• Density: 1.37g/cm³
• Vapor Pressure: 1.08E-12mmHg at 25°C
• Refractive Index: 1.628
• CAS DataBase Reference: N-[2-(2,4-dichlorophenoxy)ethyl]-1-benzofuran-2-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[2-(2,4-dichlorophenoxy)ethyl]-1-benzofuran-2-carboxamide(5927-94-6)
• EPA Substance Registry System: N-[2-(2,4-dichlorophenoxy)ethyl]-1-benzofuran-2-carboxamide(5927-94-6)

Safety Data

• Hazardous Substances Data: 5927-94-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 19598-15-3 trans-1,2-bromoindane 
• 95-13-6 1-indene 
• 28078-73-1 methyl hypobromite 
• 79-21-0 peracetic acid 

Relevant articles and documents

Diastereoselective Synthesis of Cyclic sp 3 -Enriched cis -β-Alkoxysulfonyl Chlorides

A three-step synthesis of β-alkoxy-substituted alicyclic sulfonyl chlorides from cyclic alkenes and alcohols is reported. The scope of the method was studied for a range of the substrates with various steric and electronic properties. The title compounds were obtained on a hundred-gram scale in up to 52% overall yield scale as single cis -diastereomers.

BNBTS More than brominating agent: Green and one-pot route for the C-N bond formation in water from alkenes

In this paper, in addition to introducing efficient method for bromohydrin and bromoether preparation, simple, green and efficient method to C-N bond formation from alkene and N,N'-Dibromo-N,N'-1,2-ethanediyl- bis(ptoluenesulfonamide) [BNBTS] in water was investigated. The reaction between alkenes, β-cyclodexterin, and BNBTS took place in water afterward, by making media basic; it will give the corresponding valuable building blocks in good yields (45-79%).

Organocatalysis in the stereoselective bromohydrin reaction of alkenes

An efficient regio- and stereo-selective (>99:1) trans-bromohydrination (bromohydroxylation and bromomethoxylation) of alkenes including α,β-unsaturated carbonyl compounds with N-bromosuccinimide (NBS) has been achieved by using 1.0 mol% of N,N'-diarylthi