Date published: 2025-10-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

Methyl 4-(4-bromophenyl)-4-oxobutanoate (CAS 30913-86-1)

0.0(0)
Write a reviewAsk a question

CAS Number:
30913-86-1
Molecular Weight:
271.11
Molecular Formula:
C11H11BrO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Methyl 4-(4-bromophenyl)-4-oxobutanoate functions as a reagent in organic synthesis. It acts as an acylating agent in the formation of esters and amides, playing a role in the modification of organic molecules. Methyl 4-(4-Bromophenyl)-4-Oxobutanoate participates in acylation reactions, where it adds an acyl group to other compounds, leading to the formation of new chemical entities. Through its acylating properties, it facilitates the creation of diverse molecular structures, contributing to the development of novel compounds in development. At the molecular level, Methyl 4-(4-bromophenyl)-4-oxobutanoate undergoes nucleophilic acylation, forming covalent bonds with other molecules and influencing their chemical properties. Its mechanism of action involves the transfer of its acyl group to specific functional groups within organic molecules, enabling the synthesis of complex chemical structures for experimental purposes.


Methyl 4-(4-bromophenyl)-4-oxobutanoate (CAS 30913-86-1) References

  1. Cross metathesis of allyl alcohols: how to suppress and how to promote double bond isomerization.  |  Schmidt, B. and Hauke, S. 2013. Org Biomol Chem. 11: 4194-206. PMID: 23676990
  2. Biocatalytic Asymmetric Reduction of γ-Keto Esters to Access Optically Active γ-Aryl-γ-butyrolactones  |  Borowiecki, P., Telatycka, N., Tataruch, M., Żądło‐Dobrowolska, A., Reiter, T., Schühle, K.,.. & Kroutil, W. 2020. Advanced Synthesis & Catalysis. 362(10): 2012-2029.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl 4-(4-bromophenyl)-4-oxobutanoate, 1 g

sc-337971
1 g
$235.00