Epoxy curing agent Knowledge phenyl benzoate

phenyl benzoate

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Phenyl benzoate structural formula

Structural formula

Business number 0270
Molecular formula C13H10O2
Molecular weight 198.22
label

phenyl benzoate,

phenyl benzoate,

Benzoic acid phenyl ester,

C6H5CO2C6H5

Numbering system

CAS number:93-99-2

MDL number:MFCD00003072

EINECS number:202-293-2

RTECS number:DH6299500

BRN number:1566346

PubChem number:24847623

Physical property data

1. Properties: colorless prismatic crystals. It smells like grass oil.

2. Relative density (20℃, 4℃): 1.235

3. Relative density (25℃, 4℃): 1.041131

4. Melting point (ºC): 71

5. Boiling point (ºC, normal pressure): 314

6. Boiling point (ºC, 2.0kpa): 314℃

7. Refractive index at room temperature (n20): 1.550280

8. Refractive index at room temperature (n 25): 1.5403102

9. Specific rotation (º): Undetermined

10. Gas phase standard heat of combustion (enthalpy) (kJ·mol-1): -6402.2

11. The gas phase standard claims heat (enthalpy) (kJ·mol-1): -142.6

12. The standard heat of combustion (enthalpy) of the crystal phase (kJ·mol-1): -6303.2

13. The standard claim heat of the crystal phase ( Enthalpy) (kJ·mol-1): -241.6

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa) : Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V/V): Undetermined

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18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Easily soluble in hot ethanol, slightly soluble in cold ethanol and ether, insoluble in water.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 57.89

2. Molar volume (cm3/mol): 172.8

3. Isotonic specific volume (90.2K ): 444.6

4. Surface tension (dyne/cm): 43.8

5. Polarizability (10-24cm3): 22.95

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 26.3

7.Number of heavy atoms���:15

8. Surface charge: 0

9. Complexity: 201

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None yet

Storage method

This product should be kept sealed.

Synthesis method

Obtained from the reaction of benzoyl chloride and phenol. Dissolve phenol in pyridine, add benzoyl chloride dropwise, control the temperature not to exceed 50°C, complete the addition, and react at 120°C for 30 minutes. After cooling, add water to precipitate crystals, filter, wash and dry to obtain phenyl benzoate. The yield is 93%. The above-mentioned acylation reaction can also be carried out by reacting phenol sodium salt solution and benzoyl chloride at room temperature for 0.5 hours. After filtering and washing with water, phenyl benzoate can be obtained. For refinement, ethanol recrystallization can be used, and the yield is 75-80%.

Purpose

This product is heated to 130°C in the presence of aluminum trichloride and rearranged to form 4-hydroxybenzophenone, which is used as an intermediate in organic synthesis and in the production of pharmaceuticals and other products.

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