Date published: 2025-10-18

1-800-457-3801

SCBT Portrait Logo
Seach Input

4-Iodobutyric acid (CAS 7425-27-6)

0.0(0)
Write a reviewAsk a question

CAS Number:
7425-27-6
Molecular Weight:
214.00
Molecular Formula:
C4H7IO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-Iodobutyric acid is frequently in organic synthesis and biochemistry due to its reactivity and utility as a building block for more complex molecules. It serves as a versatile reagent in the preparation of various organic compounds, including the synthesis of gamma-lactones and modification of peptides and proteins. 4-Iodobutyric acid is involved in the study of alkylation reactions where the iodine atom acts as a good leaving group, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. This reactive intermediate is also in the conjugation of small molecules to proteins or other macromolecules, which can be for the study of molecular interactions and functions. The iodine atom of 4-Iodobutyric acid provides a reactive site for further functionalization, which is applied in the design of new molecules.


4-Iodobutyric acid (CAS 7425-27-6) References

  1. Study of the quantitative structure-mobility relationship of carboxylic acids in capillary electrophoresis based on support vector machines.  |  Xue, CX., et al. 2004. J Chem Inf Comput Sci. 44: 950-7. PMID: 15154762
  2. Antiproliferative and phenotype-transforming antitumor agents derived from cysteine.  |  Glenn, MP., et al. 2004. J Med Chem. 47: 2984-94. PMID: 15163181
  3. Prediction of the electrophoretic mobilities of some carboxylic acids from theoretically derived descriptors.  |  Fatemi, MH. 2004. J Chromatogr A. 1038: 231-7. PMID: 15233538
  4. Enhancing electrospray ionization efficiency of peptides by derivatization.  |  Mirzaei, H. and Regnier, F. 2006. Anal Chem. 78: 4175-83. PMID: 16771548
  5. Quantitative structure-mobility relationship study of a diverse set of organic acids using classification and regression trees and adaptive neuro-fuzzy inference systems.  |  Jalali-Heravi, M. and Shahbazikhah, P. 2008. Electrophoresis. 29: 363-74. PMID: 18064595
  6. Hydroalkylation of Olefins To Form Quaternary Carbons.  |  Green, SA., et al. 2019. J Am Chem Soc. 141: 7709-7714. PMID: 31030508

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Iodobutyric acid, 1 g

sc-232785
1 g
$194.00