Alternatived Products of [ 83847-14-7 ]
Product Details of [ 83847-14-7 ]
CAS No. : | 83847-14-7 |
MDL No. : | MFCD23098829 |
Formula : |
C23H23NO5
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | LNEDNZUQKOGNLJ-UHFFFAOYSA-N |
M.W : |
393.43
|
Pubchem ID : | 640210 |
Synonyms : |
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Application In Synthesis of [ 83847-14-7 ]
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
- Downstream synthetic route of [ 83847-14-7 ]
- 1
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[ 767-00-0 ]
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[ 83883-26-5 ]
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[ 83847-14-7 ]
- 2
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[ 83847-14-7 ]
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[ 818-61-1 ]
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polymer, degree of polymerization 200, polydispersity 2; monomer(s): 2-hydroxyethyl acrylate, 10 percent; 4-(6-acryloyloxy-hexyloxy)-benzoic acid 4-cyano-phenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With 2,2'-azobis(isobutyronitrile) at 55℃; |
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- 3
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[ 83847-14-7 ]
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polymer, dispersion polymerization, colloid diameter (standard deviation) = 0.69 (0.05) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol at 75℃; for 24h; |
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- 4
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 10:1), colloid diameter (standard deviation) = 0.75 (0.05) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 5
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 4:1), colloid diameter (standard deviation) = 0.83 (0.06) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 6
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 2:1), colloid diameter (standard deviation) = 1.01 (0.08) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 7
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 1:1), colloid diameter (standard deviation) = 1.16 (0.07) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 8
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 2:3), colloid diameter (standard deviation) = 1.74 (0.75) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 9
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 1:2), colloid diameter (standard deviation) = 3.65 (2.95) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 10
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[ 83847-14-7 ]
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polymer, dispersion polymerization (in ethanol/2-methoxyethanol 1:5), colloid diameter (standard deviation) = 2.4 (1.1) μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 11
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[ 83847-14-7 ]
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polymer, dispersion polymerization, colloid diameter up to 30 μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose (Mn = 82020, Mw = 138000 g/mol); dibenzoyl peroxide In 2-methoxy-ethanol at 75℃; for 24h; |
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- 12
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[ 83847-14-7 ]
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polymer, seed polymerization, colloid diameter = 1.57 +/- 0.12 μm; monomer(s): 4-(6-acryloyloxy-hexyloxy)benzoic acid 4-cyanophenyl ester
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With hydroxypropyl cellulose; dibenzoyl peroxide In ethanol; 2-methoxy-ethanol at 75℃; for 24h; |
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- 13
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[ 2009-83-8 ]
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[ 83847-14-7 ]
Yield | Reaction Conditions | Operation in experiment |
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Multi-step reaction with 3 steps
1: 54 percent / potassium iodide, potassium hydroxide / ethanol; H2O / 20 h / Heating
2: 67 percent / hydroquinone, p-toluenesulphonic acid / benzene / 20 h / Heating
3: 1.) thionyl chloride, 2,6-di-tert-butyl-4-methyl phenol, DMF; 2.) triethylamine / 1.) 25 min; 2.) chloroform, room t., 24 h |
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- 14
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[ 83883-25-4 ]
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[ 83847-14-7 ]
Yield | Reaction Conditions | Operation in experiment |
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Multi-step reaction with 2 steps
1: 67 percent / hydroquinone, p-toluenesulphonic acid / benzene / 20 h / Heating
2: 1.) thionyl chloride, 2,6-di-tert-butyl-4-methyl phenol, DMF; 2.) triethylamine / 1.) 25 min; 2.) chloroform, room t., 24 h |
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- 15
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[ 99-96-7 ]
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[ 83847-14-7 ]
Yield | Reaction Conditions | Operation in experiment |
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Multi-step reaction with 3 steps
1: 54 percent / potassium iodide, potassium hydroxide / ethanol; H2O / 20 h / Heating
2: 67 percent / hydroquinone, p-toluenesulphonic acid / benzene / 20 h / Heating
3: 1.) thionyl chloride, 2,6-di-tert-butyl-4-methyl phenol, DMF; 2.) triethylamine / 1.) 25 min; 2.) chloroform, room t., 24 h |
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- 16
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[ 174063-87-7 ]
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C31H40O5
[ No CAS ]
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[ 83847-14-7 ]
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None
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
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With 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one In cyclohexanone; toluene UV-irradiation; |
1
A solid, in which 40 % by weight of the compound of the Formula 1, 27 % by weight of the compound of the Formula 2, 27 % by weight of the compound of the Formula 3, and 6.0 % by weight of Irgacure907 (manufactured from the company Ciba-Geigy, Switzerland) were mixed, was dissolved in a mixed solvent including 70 % by weight of toluene and 30 % by weight of cyclohexanone so that content of the solid can be 25 % by weight, to prepare a polymerizable and reactive liquid crystalline EPO mixture solution.[110] A fluorocarbon-based surfactant Novec (trade name, manufactured from the company 3M, U.S.A.) FC4430 was added to the polymerizable and reactive liquid crystalline mixture solution so that its content can be 1.0 % by weight, based on 100 % by weight of the solid included in the entire solution.[Ill] The triacetyl cellulose film (trade name: 80UZ, manufactured from the companyFuji, Japan) was corona discharge-treated, and then coated with the polymerizable and reactive liquid crystalline mixture solution including the surfactant using a wire-bar coater (No.4), kept at 50°C in a drying oven for 2 minutes, and then cured once at a rate of 3 m/min using a 80 W/cm high-pressure mercury lamp. The resultant liquid crystal film was clear and its thickness was 1.0 D. |