61485-85-6

Usage

Physical state

Colorless liquid It is a liquid at room temperature and is colorless in appearance.

Solubility

Insoluble in water 2,6-Dibromoheptane does not dissolve well in water.

Boiling point

High It has a high boiling point, which means it requires more heat to vaporize and turn into a gas.

Uses

Intermediate in synthesis It is primarily used as an intermediate in the synthesis of other organic compounds, particularly in the manufacturing of pharmaceuticals and agrochemicals.

Uses

Reagent in chemical reactions 2,6-Dibromoheptane is also used as a reagent in various chemical reactions, such as in the synthesis of polymers and in organic synthesis.

Hazardous substance

Potential health and environmental risks It is considered to be a hazardous substance and should be handled with care due to its potential negative effects on human health and the environment.

Upstream product

• 20722-53-6 1-benzoyl-2,6-dimethyl-piperidine 
• 17037-71-7 N-benzoyl-cis-2,6-dimethylpiperidine 
• 766-17-6 (2R,6S)-2,6-dimethylpiperidine 
• 72693-12-0 6-hydroxyheptan-2-one 
• 5969-12-0 heptane-2,6-diol 

Relevant academic research and scientific papers

Borane-Catalyzed Synthesis of Quinolines Bearing Tetrasubstituted Stereocenters by Hydride Abstraction-Induced Electrocyclization

The borane-catalyzed synthesis of quinoline derivatives bearing tetrasubstituted stereocenters from vinyl anilines has been developed. Mechanistic studies and quantum-mechanical investigations support the hydride abstraction/electrocyclization/hydride add

A Convenient Synthetic Route to Methylated Silacyclohexanes

The von Braun degradation of substituted piperidines is a general and economical route to a variety of substituted primary and secondary α,ω-dibromopentanes.Grignard ring closure procedures have been carried out with seven different dibromopentanes in moderate to good yields.Ring closures with MeClSiCl2 lead to product mixtures which are appreciably enriched in one isomer, affording a convenient entry into a variety of derivatives which can be used for stereochemical studies.Assignment of structures based on 1H NMR and mass spectral fragmentation patterns is discussed