≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2,2-Dimethylcyclopentanon ist ein Keton. Es wurde über die Synthese verschiedener C-2-substituierter Vitamin-D-Derivate mit einer 2,2-Dimethylcyclopentanon-Einheit in den Seitenketten berichtet. Die regioselektive Synthese von 2,2-Dimethylcyclopentanon über seinen Enolat-Vorläufer, der regioselektiv mit dem 2-Pyrrolidon-Magnesiumsalz erhalten wird, wurde berichtet.
das 2,2-Dimethylcyclopentanon-Enolat kann als Ausgangsreagenz für die enantioselektive Synthese von chiralen Phosphinen der P-Aryl-2-phosphabicyclo[3.3.0]octan-Familie (PBO) verwendet werden, und zwar für die Synthese von: . 2,6,6-Trimethyl-2-azaspiro[4.4]nonan-1,3-dion, einer Spirosuccinimid-Einheit von Asparparalin A . neuartige Spiropentanopyrrolizidin-Oxim-Alkaloide, nämlich 2′,3′,5′,6′,7′,7a′-Hexahydro-2,2-dimethylspirocyclopentan-1 . δ,δ-dimethyl-δ-valerolacton, über Baeyer-Villiger-Oxidation.
| Pubchem Sid | 504757154 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504757154 |
| Kanonisches Lächeln | CC1(CCCC1=O)C |
| IUPAC Name | 2,2-dimethylcyclopentan-1-one |
| InChIKey | FTGZMZBYOHMEPS-UHFFFAOYSA-N |
| INCHI | 1S/C7H12O/c1-7(2)5-3-4-6(7)8/h3-5H2,1-2H3 |
| Isomere SMILES | CC1(CCCC1=O)C |
| WGK Deutschland | 3 |
| UN-Nummer | 1224 |
| Molekulargewicht | 112.17 |
| Reaxy-Rn | 1853308 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1853308&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Klasse | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Ketones |
| Direct Parent | Cyclic ketones |
| Alternative Parents | Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Cyclic ketone - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety. |
| External Descriptors | Not available |
| Brechungsindex | 1.433(lit.) |
|---|---|
| Flammpunkt (°F) | 91.4 °F |
| Flammpunkt (°C) | 33 °C |
| Siedepunkt (°C) | 143-145 °C(lit.) |
| Molekulargewicht | 112.170 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 112.089 Da |
| Monoisotopic Mass | 112.089 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 8 |
| Formal Charge | 0 |
| Complexity | 114.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
B1802022