Date published: 2026-2-4

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Phthaloyl chloride (CAS 88-95-9)

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Alternate Names:
Phthaloyl dichloride
CAS Number:
88-95-9
Molecular Weight:
203.02
Molecular Formula:
C8H4Cl2O2
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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Phthaloyl chloride is used in study focused on the synthesis of aromatic dicarboxylic acids and their derivatives. It is extensively applied in studies aiming to improve polymer characteristics such as thermal stability and mechanical strength, which are for industrial applications. Phthaloyl chloride is utilized to investigate cross-linking reactions in polymers, which can enhance the material properties required for specific uses. It is involved in the study of organic synthesis, where Phthaloyl chloride acts as an acylating agent to introduce phthaloyl groups into organic molecules, aiding in the study of reaction mechanisms and product development. In the field of materials science, Phthaloyl chloride is used to modify the surface properties of various substrates to produce coatings with desired chemical and physical properties.


Phthaloyl chloride (CAS 88-95-9) References

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  2. Highly active, regioselective, and enantioselective hydroformylation with Rh catalysts ligated by Bis-3,4-diazaphospholanes.  |  Clark, TP., et al. 2005. J Am Chem Soc. 127: 5040-2. PMID: 15810837
  3. Crystal structure and identification of resonance forms of diethyl 2-(3-oxoiso-1,3-di-hydro-benzo-furan-1-yl-idene)malonate.  |  Tyumentsev, MS., et al. 2017. Acta Crystallogr E Crystallogr Commun. 73: 1576-1579. PMID: 29250385
  4. Synthesis, identification and quantification of oligomers from polyester coatings for metal packaging.  |  Pietropaolo, E., et al. 2018. J Chromatogr A. 1578: 15-27. PMID: 30314684
  5. Successively Regioselective Electrosynthesis and Electron Transport Property of Stable Multiply Functionalized [60]Fullerene Derivatives.  |  Yan, XX., et al. 2020. Research (Wash D C). 2020: 2059190. PMID: 32149279
  6. Preparation of PVA Fluorescent Gel and Luminescence of Europium Sensitized by Terbium (III).  |  Wei, Y., et al. 2020. Polymers (Basel). 12: PMID: 32290600
  7. Multi-Functional Luminescent Coating for Wood Fabric Based on Silica Sol-Gel Approach.  |  Li, M., et al. 2020. Polymers (Basel). 13: PMID: 33396910
  8. Structure-Dependent Photoluminescence of Europium(III) Coordination Oligomeric Silsesquioxane: Synthesis and Mechanism.  |  Li, M., et al. 2021. ACS Omega. 6: 227-238. PMID: 33458475
  9. Unparalleled Armour for Aramid Fiber with Excellent UV Resistance in Extreme Environment.  |  Chen, F., et al. 2021. Adv Sci (Weinh). 8: 2004171. PMID: 34194929
  10. Efficient Synthesis of Novel Plasticizers by Direct Palladium-Catalyzed Di- or Multi-carbonylations.  |  Hu, Y., et al. 2023. Angew Chem Int Ed Engl. 62: e202214706. PMID: 36468459
  11. Reversal of Multidrug Resistance by Symmetrical Selenoesters in Colon Adenocarcinoma Cells.  |  Rácz, B., et al. 2023. Pharmaceutics. 15: PMID: 36839934
  12. One out of Four: Kinetic Resolution of Stereoisomeric Mixtures of Secondary Alcohols with a Quaternary Carbon Atom in the β-Position by Cu-H-Catalyzed Enantioselective Silylation.  |  Papadopulu, Z., et al. 2022. ACS Org Inorg Au. 2: 164-168. PMID: 36855454
  13. Simultaneous Ring Contraction and Expansion Reaction: Electrosynthesis of Heterocycle-Fused Fulleroids and Photovoltaic Application.  |  Yin, ZC., et al. 2023. Angew Chem Int Ed Engl. 62: e202304321. PMID: 37099448

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Phthaloyl chloride, 100 g

sc-250717
100 g
$83.00