1187647-98-8

Basic information

• Product Name: 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane
• Synonyms: 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane
• CAS NO: 1187647-98-8
• Molecular Weight: 263.518
• Mol File: 1187647-98-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane(1187647-98-8)
• EPA Substance Registry System: 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane(1187647-98-8)

Safety Data

• Hazardous Substances Data: 1187647-98-8(Hazardous Substances Data)

Usage

General Description

2-(2-bromo-5-chlorophenyl)-1,3-dioxolane is a chemical compound with the molecular formula C8H6BrClO2. It is a cyclic organic compound with a dioxolane ring and bromine and chlorine substituents on the phenyl group. This chemical is used in various industrial applications, including as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as a reagent in organic synthesis to introduce the 1,3-dioxolane moiety into different molecules. Additionally, 2-(2-bromo-5-chlorophenyl)-1,3-dioxolane may have potential applications in the field of materials science and biotechnology. However, it is important to handle this chemical with caution and follow proper safety protocols due to its potential hazards.

Upstream product

• 174265-12-4 2-bromo-5-chlorobenzaldehyde 
• 107-21-1 ethylene glycol 
• 107-07-3 2-chloro-ethanol 

Downstream Products

• 1187649-62-2 1-(4-chloro-2-(1,3-dioxolan-2-yl)phenyl)-1H-imidazole 
• 1426687-92-4 4-chloro-N-(7-chloro-2-cyclohexyl-3-oxo-2,3-dihydroisoquinolin-4-yl)-N-phenylbenzamide 
• 1426687-94-6 N-(7-chloro-3-oxo-2-propyl-2,3-dihydroisoquinolin-4-yl)-N-(prop-2-ynyl)benzamide 
• 1426688-35-8 4-(7-chloro-2-cyclohexyl-3-oxo-2,3-dihydroisoquinolin-4-yl)-7-methoxy-3, 4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione 
• 1426688-47-2 4-chloro-2-(1,3-dioxolan-2-yl)benzaldehyde 
• 1187647-99-9 5-chloro-2-(1H-imidazol-1-yl)benzaldehyde 
• 1443497-73-1 2-allyl 5-chlorobenzaldehyde 

Relevant articles and documents

Asymmetric domino multicatalysis for the synthesis of 3-substituted phthalides: Cinchonine/nhc cooperative system

It is demonstrated that two organocatalysts, achiral NHC and chiral bifunctional cinchonine, are mutually compatible and operating concurrently and effectively to promote the asymmetric domino oxidation/oxa-Michael addition reaction. This protocol allowed

Efficient synthesis of dibenzazepine lactams via a sequential Pd-catalyzed amination and aldol condensation reaction

A simple and efficient reaction was developed for the synthesis of dibenzazepine lactam derivatives. The core 7-membered azepine ring was formed by a stepwise sequence involving a palladium-catalyzed amination and an aldol condensation.

Enantioselective N-Heterocyclic Carbene Catalysis by the Umpolung of α,β-Unsaturated Ketones

N-Heterocyclic carbene-catalyzed formation of β-anionic intermediates from enones has been employed in the enantioselective synthesis of 2-aryl propionates. The reaction was achievable using a homochiral 4-MeOC6H4 morpholinone cataly