4-Chlorophthalic anhydride
4-Chlorophthalic anhydride
  • CAS No.:118-45-6
Other grades of this product :
4-Chlorophthalic anhydride Basic information
Product Name:4-Chlorophthalic anhydride
Synonyms:4-CHLOROPHTHALIC ACID ANHYDRIDE;4-CHLOROPHTHALIC ANHYDRIDE;CHLOROPHTHALIC ANHYDRIDE;Chlorophtalicanhydre,95%;ChlorophthalicAnhydride,4-;4-Chlorophthalic;5-Chloroisobenzofuran-1,3-dione;4-CHLOROPHTHALIC ANHYDRIDE 95+%
CAS:118-45-6
MF:C8H3ClO3
MW:182.56
EINECS:204-251-9
Product Categories:API Intermediate;Anhydride;Acids and Derivatives;Phthalic Acids, Esters and Derivatives
Mol File:118-45-6.mol
4-Chlorophthalic anhydride Chemical Properties
Melting point 96°C
Boiling point 290 °C
density 1.594±0.06 g/cm3(Predicted)
vapor pressure 0.058-0.058Pa at 25℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Toluene
form Solid:particulate/powder
color White to Almost white
LogP2.713
CAS DataBase Reference118-45-6(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 2932990090
MSDS Information
4-Chlorophthalic anhydride Usage And Synthesis
Uses4-chlorophthalic anhydride is an important monomer synthesis of polyimide and polyimide is considered to be the highest tolerance has been industrialized in the polymer and the shape and chemical stability of other materials can not like the outburst strength, wear resistance and extreme temperatures, excellent, has been widely used in aviation, aerospace, microelectronics and atom to the field of high technology. 4- of 4-chlorophthalic anhydride is mainly used in the synthesis of diphenyl ether dianhydride anhydride, two single and two double ether, thioether dianhydride anhydride two, two, and two amine polymerization ring was a series of polyimide engineering plastic with excellent performance. 4- of 4-chlorophthalic anhydride is not only the ideal raw material for the synthesis of various intermediates of polyimide, and can be used as a drug or pesticide.
Synthesis Reference(s)Tetrahedron Letters, 23, p. 371, 1982 DOI: 10.1016/S0040-4039(00)86833-1

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