2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)] | CAS No. 181028-79-5

2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)]

Basic Information

CAS Number

181028-79-5

Molecular Formula

C15H18O8P2

Molecular Weight

388.25 g/mol

AD

Basic Physical Properties

CC(C)(C1=CC=C(C=C1)OP(=O)(O)O)C2=CC=C(C=C2)OP(=O)(O)O

InChI

InChI=1S/C15H18O8P2/c1-15(2,11-3-7-13(8-4-11)22-24(16,17)18)12-5-9-14(10-6-12)23-25(19,20)21/h3-10H,1-2H3,(H2,16,17,18)(H2,19,20,21)

InChIKey

LAUIXFSZFKWUCT-UHFFFAOYSA-N

LogP

2.9555000000000025

Topological Polar Surface Area

133.52 Ų

Hydrogen Bond Donor/Acceptor

4 / 8

Complexity

478

Synonyms & References

English

  • Bisphenol A diphosphate
  • SCHEMBL1815086
  • 181028-79-5
  • 75805-15-1
  • NS00019787
  • [4-[2-(4-phosphonooxyphenyl)propan-2-yl]phenyl] dihydrogen phosphate
  • Propane-2,2-diylbis(4,1-phenylene) bis(dihydrogen phosphate)
  • Bisphenyl A Bis(diphenyl phosphate)
  • BDP
  • Biphenol A Diphosphate
  • 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol,phosphono dihydrogen phosphate
  • BDP (BIPHENOL A DIPHOSPHATE)
  • Bisphenol A bis(diphenyl)phosphate, Rx product of Phosphoric trichloride, biphenol A and phenol
  • Bisphenol A bis(diphenyl)phosphate, Rx product of Phosphoric trichloride, biphenol A and phenolneat
  • Phosphoric trichloride,reaction products with bisphenol A and phenol
  • DRIL2
  • ARID3B
  • Bright and dead ringer protein
  • BISPHENOL A BIS(DIPHENYL PHOSPHATE) (BDP)
  • AT-rich interactive domain-containing protein 3B
  • ANTI-BDP (ARID3B)(C-TERMINAL) antibody produced in rabbit
  • Reaktionsprodukt von Phosphortrichlorid, Bisphenol A und Phenol

MDL Number

MFCD09752835

FAQ

What are the physical and chemical properties of 2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)] (CAS: 181028-79-5)?

The compound has a crystalline form and a molecular weight of approximately 274.14 g/mol. It shows good solubility in polar solvents like water and dimethylformamide. Chemically, it exhibits reactivity towards nucleophiles and can be used as a phosphate donor. It is stable under normal conditions but decomposes at high temperatures.

How is 2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)] (CAS: 181028-79-5) typically synthesized?

This compound can be synthesized by the esterification of a phenol with a diester of a dicarboxylic acid followed by a nucleophilic substitution reaction. Common catalysts include sulfuric acid or tosyl chloride, with yields up to 90% and good selectivity.

What industries use 2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)] (CAS: 181028-79-5)?

This compound is used in pharmaceuticals for its role as a phosphate donor in certain therapeutic applications. It is also employed in polymer chemistry for the modification of polymer properties and in the development of sensors and semiconductors.

What precautions should be taken when handling 2,2-Propanediyldi-4,1-phenylene bis[dihydrogen (phosphate)] (CAS: 181028-79-5)?

When handling this compound, use appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Perform reactions in a well-ventilated area or a fume hood. Dispose of waste materials according to local regulations. Always refer to the Safety Data Sheet (SDS) for detailed safety information and emergency procedures.

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