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Phthaloyl chloride, 94%, Thermo Scientific Chemicals
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化學識別
CAS88-95-9
IUPAC Namebenzene-1,2-dicarbonyl dichloride
Molecular FormulaC8H4Cl2O2
InChI KeyFYXKZNLBZKRYSS-UHFFFAOYSA-N
SMILESClC(=O)C1=CC=CC=C1C(Cl)=O
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規格表Phthaloyl chloride is used for the preparation of volatile acid chlorides from the acids. It acts as a trapping agent for the nitrite ion in the fluorodenitration of aromatic substrates with potassium fluoride. It serves as an additive in polymers and fibers to improve the color stability. It is used as an ingredient in ceramic mold binders, as a stabilizer for polymers and in reverse osmosis membranes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Phthaloyl chloride is used for the preparation of volatile acid chlorides from the acids. It acts as a trapping agent for the nitrite ion in the fluorodenitration of aromatic substrates with potassium fluoride. It serves as an additive in polymers and fibers to improve the color stability. It is used as an ingredient in ceramic mold binders, as a stabilizer for polymers and in reverse osmosis membranes.
Solubility
Miscible with ether.
Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with water, alcohols oxidizing agents and strong bases.
Phthaloyl chloride is used for the preparation of volatile acid chlorides from the acids. It acts as a trapping agent for the nitrite ion in the fluorodenitration of aromatic substrates with potassium fluoride. It serves as an additive in polymers and fibers to improve the color stability. It is used as an ingredient in ceramic mold binders, as a stabilizer for polymers and in reverse osmosis membranes.
Solubility
Miscible with ether.
Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with water, alcohols oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Can be used for the preparation of volatile acid chlorides from the acids by exchange and distillation of the product from the reaction medium; see, e.g.: Org. Synth. Coll., 3, 422 (1955). For a one step conversion of ethyl esters to the corresponding acid chlorides, with loss of ethyl chloride, see: J. Org. Chem., 44, 2291 (1979).
- Acts as a trap for the nitrite ion in the fluorodenitration of aromatic substrates with Potassium fluoride, 14130: Chem. Lett., 2213 (1989); J. Org. Chem., 56, 6406 (1991).
- Nicolaou, K. C.; Lu, Z.; Li, R.; Woods, J. R.; Sohn, T. I. Total Synthesis of Shishijimicin A. J. Am. Chem. Soc. 2015, 137 (27), 8716-8719.
- Zahmatkesh, S.; Dindarlooiyan, N. Poly (azo-ester) s: Interfacial Synthesis of Optically Active Polymers. Lett. Org. Chem. 2015, 12 (2), 141-145.