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BENZYL PHENYL CARBONATE 97

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Products Intro: Product Name:BENZYL PHENYL CARBONATE 97
CAS:28170-07-2
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Products Intro: Product Name:Benzyl phenyl carbonate
CAS:28170-07-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-57028
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CAS:28170-07-2
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Products Intro: Product Name:Benzyl Phenyl Carbonate
CAS:28170-07-2
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Products Intro: Product Name:benzyl phenyl carbonate
CAS:28170-07-2

BENZYL PHENYL CARBONATE 97 manufacturers

BENZYL PHENYL CARBONATE 97 Basic information
Product Name:BENZYL PHENYL CARBONATE 97
Synonyms:BENZYL PHENYL CARBONATE 97;Carbonic Acid Benzyl Phenyl Ester;Benzyl phenyl carbonate 97%;Phenyl benzyl carbonate;Benzyl phenyl carbonate≥ 98%(GC);Benzyl Phenyl Carbonate >;Carbonic acid, phenyl phenylmethyl ester
CAS:28170-07-2
MF:C14H12O3
MW:228.24
EINECS:
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Mol File:28170-07-2.mol
BENZYL PHENYL CARBONATE  97 Structure
BENZYL PHENYL CARBONATE 97 Chemical Properties
Boiling point 120-130 °C0.5 mm Hg(lit.)
density 1.156 g/mL at 25 °C(lit.)
refractive index n20/D 1.5490(lit.)
Fp >230 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form clear liquid
color Colorless to Almost colorless
InChI1S/C14H12O3/c15-14(17-13-9-5-2-6-10-13)16-11-12-7-3-1-4-8-12/h1-10H,11H2
InChIKeySNGLYCMNDNOLOF-UHFFFAOYSA-N
SMILESO=C(OCc1ccccc1)Oc2ccccc2
Safety Information
Hazard Codes Xi
Risk Statements 41-43
Safety Statements 26-36/37/39
WGK Germany 3
HS Code 29209090
Storage Class12 - Non Combustible Liquids
Hazard ClassificationsEye Dam. 1
Skin Sens. 1
MSDS Information
BENZYL PHENYL CARBONATE 97 Usage And Synthesis
Chemical PropertiesColorless to clear yellow liquid
UsesBenzyl phenyl carbonate can be used to synthesize carbamate protected polyamines.
General DescriptionBenzyl phenyl carbonate can be synthesized by reacting phenyl chloroformate with benzyl alcohol in the presence of pyridine.
Synthesis
Phenyl chloroformate

1885-14-9

BENZYL PHENYL CARBONATE  97

28170-07-2

Synthesis of benzyl phenyl carbonate (Synthesis, 2002, 15, 2195-2202) Benzyl alcohol (10.8 g, 100.0 mmol) was dissolved in 100 mL of dichloromethane (CH2Cl2). After the solution was cooled to 0°C, phenyl chloroformate (15.7 g, 100 mmol) was added slowly and dropwise. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, 100 mL of water (H2O) was added, followed by washing twice with 100 mL of 2 M sulfuric acid (H2SO4). The organic phase was separated and dried over anhydrous sodium sulfate (Na2SO4). The solvent was removed by distillation under reduced pressure to give the colorless liquid product benzyl phenyl carbonate (22.5 g, 99% yield). The product was characterized by 1H NMR (CDCl3, 300 MHz): δ= 7.45-7.31 (m, 6H, arylhydrogen), 7.25-7.14 (m, 4H, arylhydrogen), 5.25 (s, 2H, benzylhydrogen).

References[1] Patent: US2013/203960, 2013, A1. Location in patent: Page/Page column
[2] Patent: US2009/36353, 2009, A1
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