Date published: 2025-11-22

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(Bromomethyl)cyclohexane (CAS 2550-36-9)

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Alternate Names:
Cyclohexylmethyl bromide
CAS Number:
2550-36-9
Purity:
99%
Molecular Weight:
177.08
Molecular Formula:
C7H13Br
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(Bromomethyl)cyclohexane is a cyclic compound comprising a single six-carbon atom ring, where one of the carbons is substituted with a bromomethyl group. This colorless liquid is extensively utilized in the chemical industry as both a solvent and a starting material for synthesizing diverse compounds. Moreover, BMC finds substantial application in laboratory experiments, contributing to a broad range of scientific research. The unique properties of (Bromomethyl)cyclohexane make it highly valuable in scientific investigations. Its excellent solvent capabilities for various organic compounds render it useful in chromatography, extraction, and synthesis procedures. The precise mechanism of action of (Bromomethyl)cyclohexane is not yet fully comprehended. However, it is believed that the bromomethyl group present in the compound contributes to its unique characteristics. This highly reactive group is thought to engage in covalent bond formation with other molecules, such as proteins. This interaction potentially underlies (Bromomethyl)cyclohexane′s ability to affect various biochemical processes.


(Bromomethyl)cyclohexane (CAS 2550-36-9) References

  1. Synthesis, bioactivity, 3D-QSAR studies of novel dibenzofuran derivatives as PTP-MEG2 inhibitors.  |  Ma, Y., et al. 2017. Oncotarget. 8: 38466-38481. PMID: 28388567
  2. Transition-metal-free one-pot synthesis of alkynyl selenides from terminal alkynes under aerobic and sustainable conditions.  |  Heredia, AA. and Peñéñory, AB. 2017. Beilstein J Org Chem. 13: 910-918. PMID: 28684972
  3. Exploration of Novel Chemical Space: Synthesis and in vitro Evaluation of N-Functionalized Tertiary Sulfonimidamides.  |  Izzo, F., et al. 2018. Chemistry. 24: 9295-9304. PMID: 29726583
  4. Migratory functionalization of unactivated alkyl bromides for construction of all-carbon quaternary centers via transposed tert-C-radicals.  |  Zhu, C., et al. 2020. Nat Commun. 11: 4860. PMID: 32978381
  5. Comprehensive Protocol for the Identification and Characterization of New Psychoactive Substances in the Service of Law Enforcement Agencies.  |  Bulska, E., et al. 2020. Front Chem. 8: 693. PMID: 33102427
  6. A Widely Applicable Dual Catalytic System for Cross-Electrophile Coupling Enabled by Mechanistic Studies.  |  Charboneau, DJ., et al. 2020. ACS Catal. 10: 12642-12656. PMID: 33628617
  7. Structure Activity Relationship of N-Substituted Phenyldihydropyrazolones Against Trypanosoma cruzi Amastigotes.  |  Sijm, M., et al. 2021. Front Chem. 9: 608438. PMID: 33996737
  8. Design, Synthesis, and Biological Evaluation of Novel 6H-Benzo[c]chromen-6-one Derivatives as Potential Phosphodiesterase II Inhibitors.  |  Tang, L., et al. 2021. Int J Mol Sci. 22: PMID: 34073595
  9. Design, synthesis, and biological evaluation of novel urolithins derivatives as potential phosphodiesterase II inhibitors.  |  Tang, L., et al. 2021. Sci Rep. 11: 23792. PMID: 34893678
  10. Synthesis, functionalization, and isolation of planar-chiral pillar[5]arenes with bulky substituents using a chiral derivatization agent.  |  Al-Azemi, TF., et al. 2019. RSC Adv. 9: 23295-23301. PMID: 35514477
  11. The novel visual cycle inhibitor (±)-RPE65-61 protects retinal photoreceptors from light-induced degeneration.  |  Wang, Y., et al. 2022. PLoS One. 17: e0269437. PMID: 36227868
  12. Organocatalyzed enantio- and diastereoselective isomerization of prochiral 1,3-cyclohexanediones into nonalactones bearing distant stereocenters.  |  d'Aleman, A., et al. 2023. Chem Sci. 14: 2107-2113. PMID: 36845928
  13. Nemacol is a small molecule inhibitor of C. elegans vesicular acetylcholine transporter with anthelmintic potential.  |  Harrington, S., et al. 2023. Nat Commun. 14: 1816. PMID: 37002199

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(Bromomethyl)cyclohexane, 5 g

sc-239427
5 g
$22.00

(Bromomethyl)cyclohexane, 25 g

sc-239427A
25 g
$68.00