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1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene

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1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene Basic information

Product Name:
1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene
Synonyms:
  • 1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-Methylbenzene 4-(3-Acryloyloxypropyloxy)-benzoesure -2-Methyl-1, 4-phenylester
  • 2-Methyl-1,4-phenylene-bis[4[3(acryloyloxy)propyloxy]benzoate]
  • 4-(3-Acryloyloxypropyloxy)benzoic acid 2-methyl-1,4-phenylene ester
  • 2-Methyl-1,4-phenylene bis(4-(3-(acryloyloxy)propoxy)benzoate)
  • Benzoic acid, 4-[3-[(1-oxo-2-propenyl)oxy]propoxy]-,2-methyl-1,4-phenylene ester
  • 4- (3-acryloyloxy-propoxy) benzoic acid 2-methyl-1,4-phenylene ester
  • 1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenze
  • 4-(3-Acryloyloxypropyloxy)-benzoesure 2-methyl-1, 4-phenylester
CAS:
174063-87-7
MF:
C33H32O10
MW:
588.6
EINECS:
425-560-7
Mol File:
174063-87-7.mol
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1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene Chemical Properties

Boiling point:
733.5±60.0 °C(Predicted)
Density 
1.219
vapor pressure 
0.003Pa at 25℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder
color 
White
Water Solubility 
5.3μg/L at 20℃
LogP
5.3 at 40℃
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Safety Information

HS Code 
2917399590
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1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene Usage And Synthesis

Chemical Properties

White to Almost white powder to crystal

Application

1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene is one of numerous organic compounds composing American Elements's comprehensive catalog of life science products.

Flammability and Explosibility

Not classified

Synthesis

The synthesis of 1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene is as follows:Stirrer, was added methanesulfonyl chloride 5.00 g (43.6 mmol) and tetrahydrofuran 10mL the reactor having a thermometer and two dropping device. Ice-cold while each by dropping a tetrahydrofuran solution 30mL of formula tetrahydrofuran solution 60mL and triethylamine 5.25g of (I-3-1) represented by the compound 12.9g (44.1 mmol) of (51.9 mmol) from device (equation (solution of the compound represented by I-3-1)) :( triethylamine solution) = 2: were added dropwise simultaneously with one of the drip rate.After stirring for 1 hour while cooling with ice, it was added 4-dimethylaminopyridine 2.64 g (21.6 mmol) and 2- (4-hydroxyphenyl) ethanol 2.69 g (19.4 mmol).With ice-cooling was added dropwise triethylamine 5.25g (51.9 mmol).After stirring for 7 hours, the solvent was distilled off and treated added for liquid separation dichloromethane and 5% hydrochloric acid.After the organic layer was washed with brine neutralization, and purified by column chromatography (silica gel) and reprecipitated (dichloromethane / methanol) to give the compound 12.2g of formula (I-3).82% yield, had a purity of 99.63%.

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