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{{Short description|Chemical compound}} | |||
{{Use dmy dates|date=September 2022}} | |||
{{Chembox | {{Chembox | ||
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| verifiedrevid = |
| verifiedrevid = 477209762 | ||
| ImageFile = DMPA.png | | ImageFile = DMPA.png | ||
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| ImageSize = 200px | ||
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| ImageAlt = | ||
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| PIN = 2,2-Dimethoxy-1,2-diphenylethan-1-one | ||
⚫ | | OtherNames = 2,2-Dimethoxy-2-phenylacetophenone<br />α,α-Dimethoxy-α-phenylacetophenone<br />Benzil α,α-dimethyl acetal | ||
| PIN = | |||
⚫ | |Section1={{Chembox Identifiers | ||
⚫ | | OtherNames = α,α-Dimethoxy-α-phenylacetophenone |
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⚫ | | Abbreviations = DMPA | ||
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⚫ | | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ||
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| ChemSpiderID = 81777 | | ChemSpiderID = 81777 | ||
| InChI = 1/C16H16O3/c1-18-16(19-2,14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,1-2H3 | | InChI = 1/C16H16O3/c1-18-16(19-2,14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,1-2H3 | ||
| InChIKey = KWVGIHKZDCUPEU-UHFFFAOYAK | | InChIKey = KWVGIHKZDCUPEU-UHFFFAOYAK | ||
| ChEMBL_Ref = {{ebicite| |
| ChEMBL_Ref = {{ebicite|correct|EBI}} | ||
| ChEMBL = 364734 | | ChEMBL = 364734 | ||
| StdInChI_Ref = {{stdinchicite| |
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | ||
| StdInChI = 1S/C16H16O3/c1-18-16(19-2,14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,1-2H3 | | StdInChI = 1S/C16H16O3/c1-18-16(19-2,14-11-7-4-8-12-14)15(17)13-9-5-3-6-10-13/h3-12H,1-2H3 | ||
| StdInChIKey_Ref = {{stdinchicite| |
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | ||
| StdInChIKey = KWVGIHKZDCUPEU-UHFFFAOYSA-N | | StdInChIKey = KWVGIHKZDCUPEU-UHFFFAOYSA-N | ||
| CASNo_Ref = {{cascite|correct|CAS}} | | CASNo_Ref = {{cascite|correct|CAS}} | ||
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| CASNo = 24650-42-8 | ||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
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| UNII = 1DK0094V28 | |||
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⚫ | | PubChem = 90571 | ||
⚫ | | SMILES = O=C(c1ccccc1)C(OC)(OC)c2ccccc2 | ||
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|Section2={{Chembox Properties | ||
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| C=16 | O=3 | H=16 | ||
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| Density = | ||
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|Section3={{Chembox Hazards | ||
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⚫ | '''2,2-Dimethoxy-2-phenylacetophenone''' is a ], which is used to initialize radical ] e.g. in the preparation of ].<ref>{{Cite journal | title = Percutaneous fiber-optic sensor for chronic glucose monitoring in vivo |vauthors=Liao KC, Hogen-Esch T, Richmond FJ, Marcu L, Clifton W, Loeb GE | journal = Biosens Bioelectron | year = 2008 | volume = 23 | issue = 10 | pages = 1458–65 | doi=10.1016/j.bios.2008.01.012|pmid=18304798}}</ref> Under the influence of light the molecule will form radicals which initiate the radical polymerization. It can also be used as an initiator in the process of making an ]. | ||
⚫ | '''2,2-Dimethoxy-2-phenylacetophenone''' is a photoinitiator, which is used to |
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== References == | == References == | ||
{{reflist}} | {{reflist}} | ||
{{DEFAULTSORT:Dimethoxy-2-phenylacetophenone, 2,2-}} | {{DEFAULTSORT:Dimethoxy-2-phenylacetophenone, 2, 2-}} | ||
] | ] | ||
] | ] | ||
{{ketone-stub}} | {{ketone-stub}} |
Latest revision as of 14:26, 8 September 2022
Chemical compound
Names | |
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Preferred IUPAC name 2,2-Dimethoxy-1,2-diphenylethan-1-one | |
Other names
2,2-Dimethoxy-2-phenylacetophenone α,α-Dimethoxy-α-phenylacetophenone Benzil α,α-dimethyl acetal | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
Abbreviations | DMPA |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.042.154 |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C16H16O3 |
Molar mass | 256.301 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
2,2-Dimethoxy-2-phenylacetophenone is a photoinitiator, which is used to initialize radical polymerization e.g. in the preparation of acrylate polymers. Under the influence of light the molecule will form radicals which initiate the radical polymerization. It can also be used as an initiator in the process of making an integrated circuit.
References
- Liao KC, Hogen-Esch T, Richmond FJ, Marcu L, Clifton W, Loeb GE (2008). "Percutaneous fiber-optic sensor for chronic glucose monitoring in vivo". Biosens Bioelectron. 23 (10): 1458–65. doi:10.1016/j.bios.2008.01.012. PMID 18304798.
This article about a ketone is a stub. You can help Misplaced Pages by expanding it. |