Date published: 2025-10-15

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4-Bromo-α-methylbenzyl alcohol (CAS 5391-88-8)

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CAS Number:
5391-88-8
Molecular Weight:
201.06
Molecular Formula:
C8H9BrO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Bromo-α-methylbenzyl alcohol is a compound that functions as a reagent in organic synthesis. It acts as a nucleophile in various reactions, such as nucleophilic substitution and addition reactions. The presence of the bromine atom may be a useful precursor for the synthesis of other organic compounds, particularly those that require a bromine-containing moiety. 4-Bromo-α-methylbenzyl alcohol can participate in the formation of carbon-carbon and carbon-heteroatom bonds, contributing to the construction of complex molecular structures. Its mechanism of action involves participating in chemical reactions by donating its nucleophilic functionality to form new bonds with other molecules. 4-Bromo-Å-Methylbenzyl Alcohol′s role in organic synthesis is to facilitate the creation of diverse chemical entities for further study and potential applications in various fields.


4-Bromo-α-methylbenzyl alcohol (CAS 5391-88-8) References

  1. Oxidation of Alcohols by Hydrogen Peroxide, Catalyzed by Methyltrioxorhenium (MTO): A Hydride Abstraction.  |  Zauche, TH. and Espenson, JH. 1998. Inorg Chem. 37: 6827-6831. PMID: 11670818
  2. p-Trifluoromethyldiazirinyl-etomidate: a potent photoreactive general anesthetic derivative of etomidate that is selective for ligand-gated cationic ion channels.  |  Husain, SS., et al. 2010. J Med Chem. 53: 6432-44. PMID: 20704351
  3. Chiral Crystalline Sponges for the Absolute Structure Determination of Chiral Guests.  |  Yan, K., et al. 2017. J Am Chem Soc. 139: 11341-11344. PMID: 28783333

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Bromo-α-methylbenzyl alcohol, 5 g

sc-232489
5 g
$20.00