108-85-0 | Bromocyclohexane

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$15.00	$10.00
5g	95%	in stock	$16.00	$11.00
25g	95%	in stock	$19.00	$13.00
100g	95%	in stock	$33.00	$23.00
500g	95%	in stock	$63.00	$45.00
5kg	95%	in stock	$559.00	$391.00
10kg	95%	in stock	$1,026.00	$718.00

Description

• Catalog Number: AB71606
• Chemical Name: Bromocyclohexane
• CAS Number: 108-85-0
• Molecular Formula: C6H11Br
• Molecular Weight: 163.0555
• MDL Number: MFCD00003819
• SMILES: BrC1CCCCC1
• NSC Number: 11207

Computed Properties

• Complexity: 46.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• XLogP3: 3.2

Upstream Synthesis Route

Bromocyclohexane is a versatile compound widely used in chemical synthesis as a key building block in organic reactions. It serves as an important intermediate in the preparation of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.In organic synthesis, bromocyclohexane can participate in substitution reactions to introduce a bromine atom into the carbon skeleton of organic molecules. This enables chemists to selectively modify the structure of complex compounds, allowing for the creation of new functional groups and the synthesis of novel materials.Additionally, bromocyclohexane can undergo various transformations such as nucleophilic substitution, elimination, and oxidation reactions, expanding its utility in the synthesis of diverse organic compounds. Its stability and reactivity make it a valuable reagent for preparing a wide range of chemical products with specific properties and applications in industries such as pharmaceuticals, materials science, and fine chemicals manufacturing.

Literature

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  Organic letters 20120706

• Conformational mobility of small molecules in glass-forming solutions studied by FTIR spectroscopy.

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  Chemistry (Weinheim an der Bergstrasse, Germany) 20111017

• Electrophoresis of concentrated colloidal dispersions in low-polar solvents.

  Journal of colloid and interface science 20110915

• Characterization of room temperature phosphorescence of propranolol and the chiral discrimination between R- and S-isomers.

  The Analyst 20110121

• Impact of solvent quality on nanoparticle dispersion in semidilute and concentrated polymer solutions.

  Langmuir : the ACS journal of surfaces and colloids 20101116

• Conformer-specific ionization spectroscopy of bromocyclohexane: equatorial versus axial conformers.

  The journal of physical chemistry. A 20100923

• Redesigning dehalogenase access tunnels as a strategy for degrading an anthropogenic substrate.

  Nature chemical biology 20091001

• Study of secondary relaxation in disordered plastic crystals of isocyanocyclohexane, cyanocyclohexane, and 1-cyanoadamantane.

  The Journal of chemical physics 20080907

• Chiral discrimination of quinine and quinidine based on notable room temperature phosphorescence lifetime differences with gamma-cyclodextrin as chiral selector.

  Talanta 20071031

• Isolation of axial conformers of chloro- and bromocyclohexane in a pure state as inclusion complexes with 9,9'-bianthryl, and the discovery of a novel 1,3 diaxial Cl...H weak interaction.

  Chemical communications (Cambridge, England) 20050807

• Isolation of equatorial conformers of chloro- and bromocyclohexane in a pure state as inclusion complexes with a host compound.

  Chemical communications (Cambridge, England) 20041021

• Catalytic mechanism of the maloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26.

  The Journal of biological chemistry 20031114