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℃

InChI

InChI=1S/C33H34O10/c1-4-28(34)42-20-6-18-40-25-10-14-32(15-11-25,30(36)37)24-8-9-27(23(3)22-24)33(31(38)39)16-12-26(13-17-33)41-19-7-21-43-29(35)5-2/h4-5,8-17,22H,1-2,6-7,18-21H2,3H3,(H,36,37)(H,38,39)

InChIKey

YGGIXWYFKHGVEH-UHFFFAOYSA-N

SMILES

C1(C2(=CC=C(OCCCOC(=O)C=C)C=C2)C(O)=O)=CC=C(C2(=CC=C(OCCCOC(=O)C=C)C=C2)C(O)=O)C=C1C

LogP

5.3 at 40℃

Safety Information

HS Code 

2917399590

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%.

1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene(174063-87-7)Related Product Information

• L-Alanyl-L-Glutamine
• 1,4-Bis-[4-(3-acryloyloxypropyloxy)benzoyloxy]-2-methylbenzene
• 4-(3-ACRYLOYLOXY-N-PROP-1-YLOXY)BENZOIC ACID