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About This Item
Linear Formula:
(C5H8O2)n
CAS Number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
MDL number:
SMILES string
[P](=O)(OCC)(OCC)OC(=O)\C(=N/OCC(=O)OC)\c1nc([s]c1)N
InChI
1S/C12H18N3O8PS/c1-4-21-24(18,22-5-2)23-11(17)10(8-7-25-12(13)14-8)15-20-6-9(16)19-3/h7H,4-6H2,1-3H3,(H2,13,14)/b15-10-
InChI key
DOXUHDDTLHKPOE-GDNBJRDFSA-N
form
solid
density
1.2 g/mL at 25 °C (lit.)
Quality Level
Related Categories
General description
i-PMMA can be prepared from t-C4H9MgBr. Structure of crystalline isotactic poly(methyl methacrylate) (i-PMMA) was investigated by X-ray diffraction and infra red spectroscopic techniques.
Application
The polymeric blend of isotatic (i-) poly-(methyl methacrylate) & 6,13-bis(triisopropylsilylethynyl) pentacene can be used to prepare thin films transistors (TFTs).
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Structure of isotactic poly (methyl methacrylate).
Tadokoro H, et al.
Macromolecules, 3(4), 441-447 (1970)
Self?assembled organic channel/polymer dielectric layer for organic thin?film transistor applications.
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AIP Conference Proceedings, 847, 1399-1399 (2011)
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A K Pathak et al.
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Biofilms on removable orthodontic appliances act as reservoir of microorganisms, capable of modifying the environmental condition of oral cavity and are difficult to be removed with routine hygiene measures. The present investigation includes enumeration, identification and numerical analysis of different
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Polymethylmethacrylate-graphene (PMMA/RGO) nanocomposites were prepared via in situ bulk polymerization using two different preparation techniques. In the first approach, a mixture of graphite oxide (GO) and methylmethacrylate monomers (MMA) were polymerized using a bulk polymerization method with a free radical
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