Alternatived Products of [ 2359-15-1 ]
Product Details of [ 2359-15-1 ]
CAS No. : | 2359-15-1 |
MDL No. : | MFCD00060096 |
Formula : |
C9H14N2O2
|
Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | TURITJIWSQEMDB-UHFFFAOYSA-N |
M.W : |
182.22
|
Pubchem ID : | 75381 |
Synonyms : |
|
Safety of [ 2359-15-1 ]
Signal Word: | Warning |
Class: | N/A |
Precautionary Statements: | P280-P305+P351+P338 |
UN#: | N/A |
Hazard Statements: | H302 |
Packing Group: | N/A |
GHS Pictogram: |
|
Application In Synthesis of [ 2359-15-1 ]
* 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 [ 2359-15-1 ]
- 1
-
[ 2359-15-1 ]
-
[ 3369-20-8 ]
Yield | Reaction Conditions | Operation in experiment |
|
With tetrachloromethane; bromine |
|
- 2
-
[ 2359-15-1 ]
-
2-[(methacryloylamino-methyl)-carbamoyl]-propane-1-sulfonic acid ; sodium-salt
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
With water; sodium hydrogensulfite; copper(II) sulfate |
|
- 3
-
[ 923-02-4 ]
-
[ 107-06-2 ]
-
[ 79-39-0 ]
-
[ 2359-15-1 ]
Yield | Reaction Conditions | Operation in experiment |
|
With hydrogenchloride |
|
- 4
-
[ 923-02-4 ]
-
[ 2359-15-1 ]
Yield | Reaction Conditions | Operation in experiment |
|
With hydrogenchloride |
|
- 5
-
[ 50-00-0 ]
-
[ 107-06-2 ]
-
[ 79-39-0 ]
-
[ 2359-15-1 ]
Yield | Reaction Conditions | Operation in experiment |
|
With hydrogenchloride |
|
- 6
-
[ 517-25-9 ]
-
[ 2359-15-1 ]
-
[ 100056-70-0 ]
Yield | Reaction Conditions | Operation in experiment |
|
In water |
|
- 7
-
[ 2359-15-1 ]
-
[ 7398-69-8 ]
-
polymer; monomer(s): diallyldimethylammonium chloride; N,N'-methylenebisacrylamide
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
With 2-hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone In water UV-irradiation; |
|
Yield | Reaction Conditions | Operation in experiment |
|
With dipotassium peroxodisulfate; sodium dodecyl-sulfate In water at 70℃; for 4.66667h; |
1.2
1.2. PNIPAM microgel preparation : The polymerization [20] of NIPAM was carried out in a flask equipped with a magnetic stirrer and a nitrogen feed: 3. 8 g N-isopropylacrylamide, 0.066 g N, N'-Methylenebisacrylamide and 0.15 g sodium dodecyl sulfate ("SDS") were dissolved in 240 g distilled water under continuous stirring for one hour. The solution was being nitrogen purged for 40 min before setting into a 70 °C hot bath. 0.166 g potassium persulfate, which was dissolved in 20 ml water, was then added to initiate the emulsion polymerization. The reaction last for 4 hours under nitrogen atmosphere. The reaction temperature was kept at (70+0. 5) °C. The final PNIPAM microgel size was controlled by adding different surfactant concentration: the larger the concentration, the smaller particle size. The PNIPAM micorgels were prepared with two different sizes (hydrodynamic radius Rh are 121 nm and 170 nm, respectively) for the next step IPN synthesis. [0051] All PNIPAM particles were purified via dialysis (Spectra/Por 7 dialysis membrane, MWCO 10'000, VWR) against frequent changes of stirring water for 2 weeks at room temperature. The final PNIPAM microgel concentrations were adjusted to 1.35 x10-2 g/ml. |
- 9
-
[ 106-92-3 ]
-
[ 2359-15-1 ]
-
[ 106-91-2 ]
-
[ 79-39-0 ]
-
poly(allylglycidyl ether-co-glycidyl methacrylate-co-methacrylamide-co-methylene-bismethacrylamide-co-2-trimethylammonium-ethyl methacrylate chloride)
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
|
With 4,4'-dicyano-4,4'-azo-di-valeric acid; 2-methyl-butyl acrylate; [2-(methacryloyloxy)ethyl]trimethylammonium chloride; In methanol; cyclohexane; water; at 50 - 70℃; for 6h; |
An organic solvent and 3 g of a copolymer composed of 95 parts by n-butyl methacrylate and of 5 parts of 2-trimethylammoniumethyl methacrylate chloride as protective colloid are used as initial charge in a 2 l stirred flask with thermometer, reflux condenser, nitrogen inlet tube. A monomer phase composed of diluent, and also 100 g of the monomer mixture stated in Table 1 and also 2 g of 4,4'-azobis-4-cyanovaleric acid (as polymerization initiator) are dispersed at 50 C., with stirring and nitrogen flushing, in the organic phase, and the mixture is then heated to boiling at from 65 to 70 C. The mixture is stirred for about 6 hours and then cooled to room temperature. The resultant polymer beads are isolated by suction filtration, washed, and dried in a fluidized-bed dryer. The binding capacity for penicillin amidase [U/g, moist] is then determined at various salt concentrations, and the binding yield and the swelling index [ml, moist/ml, dry] are determined. The results are collated in Table 2. |