70562-63-9

Usage

Uses

Used in Pharmaceutical Synthesis:
2-Bromo-cycloheptanone ethylene ketal serves as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications. Its unique structure allows for the creation of diverse chemical entities that can address various medical needs.
Used in Agrochemical Production:
In the agrochemical industry, 2-Bromo-cycloheptanone ethylene ketal is utilized for the synthesis of compounds that can be employed in crop protection and pest management. Its ability to participate in multiple chemical reactions aids in the creation of effective and targeted agrochemicals.
Used in Fine Chemicals Manufacturing:
2-Bromo-cycloheptanone ethylene ketal is also a key intermediate in the production of fine chemicals, which are high-purity chemicals used in various applications, including fragrances, dyes, and specialty chemicals for research purposes.
Used in Research and Development:
In the research and development sector, 2-Bromo-cycloheptanone ethylene ketal is explored for its potential in creating new organic compounds. Its reactivity and structural features make it a promising candidate for the discovery and innovation of novel chemical entities with applications in both the pharmaceutical and chemical industries.

InChI:InChI=1/C9H15BrO2/c10-8-4-2-1-3-5-9(8)11-6-7-12-9/h8H,1-7H2

Upstream product

• 107-21-1 ethylene glycol 
• 502-42-1 cycloheptanone 

Downstream Products

• 1728-24-1 1,4-dioxaspiro[4,6]undec-6-ene 
• 132113-70-3 Toluene-4-sulfonic acid 1,4-dioxa-spiro[4.6]undec-6-en-8-yl ester 
• 1194-18-9 cycloheptane-1,3-dione 

Relevant academic research and scientific papers

Optimization of Grignard ring-opening of α-brominated dioxolanes for the preparation of β-hydroxy-protected vinyl ethers by a three-step one-pot procedure

Aliphatic, cyclic, and aromatic benzoate-protected γ-hydroxy enol ethers were prepared from α-brominated dioxolanes by a three-step reaction procedure and a one-pot protocol involving Grignard reagent formation, ring-opening, and final benzoate protection

Synthesis and application of poly(diallyldimethylammonium tribromide) as a novel polymeric brominating agent

In this study, the synthesis and applications of a new supported tribromide reagent based on poly(diallyldimethylammonium chloride) is reported. This supported tribromide is used in α-bromoacetalization of ketones, bromination of alkenes and regioselective bromination of activated aromatic compounds. This method is mild and no Br2 and HBr were used. Other advantages of this reagent are stability, high efficiency, simple filtera- bility and reusability. In this study, the synthesis and applications of a new supported tribromide reagent based on poly(diallyldimethylammonium chloride) is reported. This supported tribromide is used in α-bromoacetalization of ketones, bromination of alkenes and regioselective bromination of activated aromatic compounds. This method is mild and no Br2 and HBr were used. Other advantages of this reagent are stability, high efficiency, simple filterability and reusability. Copyright

Synthetic studies on the 1-hydroxy nortropane system: An approach to Calystegines.

A general synthetic strategy for 1-hydroxy nortropane skeleton, the common feature of calystegines is described.