Diphenylmaleic anhydride

Suppliers

Names

[ CAS No. ]:
4808-48-4

[ Name ]:
Diphenylmaleic anhydride

[Synonym ]:
2,5-Furandione, 3,4-diphenyl-
Diphenylmaleic anhydride
2,3-DiphenylMaleic Anhydride
EINECS 225-370-2
3,4-diphenylfuran-2,5-dione
3,4-Diphenyl-2,5-furandione
MFCD00005521

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
437.1±45.0 °C at 760 mmHg

[ Melting Point ]:
153-157ºC

[ Molecular Formula ]:
C16H10O3

[ Molecular Weight ]:
250.249

[ Flash Point ]:
215.4±25.9 °C

[ Exact Mass ]:
250.062988

[ PSA ]:
43.37000

[ LogP ]:
3.29

[ Appearance of Characters ]:
Crystalline Powder or Powder | Yellow to dark yellow

[ Vapour Pressure ]:
0.0±1.0 mmHg at 25°C

[ Index of Refraction ]:
1.642

[ Water Solubility ]:
DMF: soluble

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2917399090

Synthetic Route

Precursor & DownStream

Precursor

  • Phenylacetic acid
  • Phenylglyoxylic acid
  • 3,4-diphenyl-5H-furan-2-one
  • diethyl (Z)-2,3-diphenylmaleate
  • 2-bromo-N-methoxy-2-phenylacetamide
  • Ethyl oxophenylacetate
  • Phenylacetyl chloride
  • Carbon dioxide
  • Diphenylacetylene

DownStream

  • 3,4-Diphenyl-1h-pyrrole-2,5-dione
  • 4,5-Diphenyl-3,6-dihydro-1,2-dithiine
  • 4,5-Diphenyl-3,6-dihydro-1,2-dithiine 1-oxide
  • phenanthro[9,10-c]furan-1,3-dione
  • 1-methyl-3,4-diphenylpyrrole-2,5-dione
  • 3,4-diphenyl-5H-furan-2-one
  • 1,5-diphenyl-3,6-dioxabicyclo[3.1.0]hexane-2,4-dione
  • 2,3-diphenylbut-2-ene-1,4-diol
  • benzoic acid

Customs

[ HS Code ]: 2917399090

[ Summary ]:
2917399090 aromatic polycarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

Sensitive enantiomeric separation of aliphatic and aromatic amines using aromatic anhydrides as nonchiral derivatizing agents.

J. Chromatogr. A. 666 , 485-491, (1994)

New pre-column derivatizing reagents: phthalic anhydride, 3-nitrophthalic anhydride, diphenic anhydride, 1,8-naphthalic anhydride and diphenylmaleic anhydride have been developed for resolving chiral ...

Comparison of the chiral separation of amino-acid derivatives by a teicoplanin and RN-beta-CD CSPs using waterless mobile phases: Factors that enhance resolution.

Chirality 16 , 318-330, (2004)

A variety of compounds containing amines (i.e., amino acids, amino alcohols, etc.) were chemically derivatized with a variety of electrophilic tagging reagents to elucidate the chiral recognition site...


More Articles


Related Compounds

  • Methacrylic anhydride
  • Perfluorooctanoic anhydride
  • DIFRUCTOSE ANHYDRIDE III
  • 2,2,3,3,4,4-Hexafluoropentanedioic Anhydride
  • acetic anhydride carbanion
  • methanesulfinic anhydride
  • 9-(3-chloro-4-pyridinyl)-3,4,6,7,9,10-hexahydro-1,8(2H,5H)-acridinedione
  • Ethyl 4-(5-(3-chloro-4-methylphenyl)-2-furyl)-6-methyl-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
  • Ethyl 4-benzyl-1-(4-chlorobenzoyl)-6,7-dimethyl-4H-pyrrolo(1,2-A)benzimidazole-3-carboxylate
  • N-(5-Chloro-2-methoxyphenyl)-2-(5,7-dichloro-1-oxoisoquinolin-2(1H)-yl)acetamide
  • Dimethyl 1-(3-chloro-2-methylphenyl)-2-methyl-1H-pyrrole-3,4-dicarboxylate
  • Ethyl 4-(3-chloropyridin-4-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
  • Methyl 2-(5-(2-chlorophenyl)furan-2-carboxamido)acetate
  • Ethyl 7-(4-bromobenzoyl)pyrrolo(1,2-B)pyridazine-5-carboxylate
  • ({6,6-Dimethylbicyclo[3.1.1]heptan-2-yl}methyl)(methyl)amine
  • 1-Methyl-2,3-dihydro-1h-indol-5-ol
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.