Date published: 2025-12-4

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cis-3-Chloroacrylic acid (CAS 1609-93-4)

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CAS Number:
1609-93-4
Purity:
≥98%
Molecular Weight:
106.51
Molecular Formula:
C3H3ClO2
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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cis-3-Chloroacrylic acid is a versatile organic acid with a wide range of scientific applications. It exhibits high water solubility and serves as a building block for numerous synthetic compounds. In addition to its role in the synthesis of dyes and catalysts, it is also actively employed in the creation of polymers, including polyurethanes and polyvinyl chloride.


cis-3-Chloroacrylic acid (CAS 1609-93-4) References

  1. Crystal structures of native and inactivated cis-3-chloroacrylic acid dehalogenase. Structural basis for substrate specificity and inactivation by (R)-oxirane-2-carboxylate.  |  de Jong, RM., et al. 2007. J Biol Chem. 282: 2440-9. PMID: 17121835
  2. Reaction mechanism of cis-3-chloroacrylic acid dehalogenase: a theoretical study.  |  Sevastik, R., et al. 2009. Biochemistry. 48: 9641-9. PMID: 19725565
  3. Crystal structures of native and inactivated cis-3-chloroacrylic acid dehalogenase: Implications for the catalytic and inactivation mechanisms.  |  Guo, Y., et al. 2011. Bioorg Chem. 39: 1-9. PMID: 21074239
  4. Characterization of a newly identified mycobacterial tautomerase with promiscuous dehalogenase and hydratase activities reveals a functional link to a recently diverged cis-3-chloroacrylic acid dehalogenase.  |  Baas, BJ., et al. 2011. Biochemistry. 50: 2889-99. PMID: 21370851
  5. Reaction of cis-3-chloroacrylic acid dehalogenase with an allene substrate, 2,3-butadienoate: hydration via an enamine.  |  Schroeder, GK., et al. 2012. J Am Chem Soc. 134: 293-304. PMID: 22129074
  6. A mutational analysis of the active site loop residues in cis-3-Chloroacrylic acid dehalogenase.  |  Schroeder, GK., et al. 2013. Biochemistry. 52: 4204-16. PMID: 23692140
  7. Reactions of Cg10062, a cis-3-Chloroacrylic Acid Dehalogenase Homologue, with Acetylene and Allene Substrates: Evidence for a Hydration-Dependent Decarboxylation.  |  Huddleston, JP., et al. 2015. Biochemistry. 54: 3009-23. PMID: 25894805
  8. Resolution of the uncertainty in the kinetic mechanism for the trans-3-Chloroacrylic acid dehalogenase-catalyzed reaction.  |  Huddleston, JP., et al. 2017. Arch Biochem Biophys. 623-624: 9-19. PMID: 28499743
  9. Kinetic and structural characterization of a cis-3-Chloroacrylic acid dehalogenase homologue in Pseudomonas sp. UW4: A potential step between subgroups in the tautomerase superfamily.  |  LeVieux, JA., et al. 2017. Arch Biochem Biophys. 636: 50-56. PMID: 29111295
  10. Structural, Kinetic, and Mechanistic Analysis of an Asymmetric 4-Oxalocrotonate Tautomerase Trimer.  |  Baas, BJ., et al. 2019. Biochemistry. 58: 2617-2627. PMID: 31074977
  11. Kinetic and Structural Analysis of Two Linkers in the Tautomerase Superfamily: Analysis and Implications.  |  Baas, BJ., et al. 2021. Biochemistry. 60: 1776-1786. PMID: 34019384
  12. Tetralone derivatives are MIF tautomerase inhibitors and attenuate macrophage activation and amplify the hypothermic response in endotoxemic mice.  |  Garai, J., et al. 2021. J Enzyme Inhib Med Chem. 36: 1357-1369. PMID: 34225560
  13. Novel Chloroflexi genomes from the deepest ocean reveal metabolic strategies for the adaptation to deep-sea habitats.  |  Liu, R., et al. 2022. Microbiome. 10: 75. PMID: 35538590

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

cis-3-Chloroacrylic acid, 1 g

sc-227663
1 g
$80.00