2,2-Dimethylcyclopentanone
2,2-Dimethylcyclopentanone structure
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Common Name | 2,2-Dimethylcyclopentanone | ||
|---|---|---|---|---|
| CAS Number | 4541-32-6 | Molecular Weight | 112.170 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 148.1±8.0 °C at 760 mmHg | |
| Molecular Formula | C7H12O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 32.8±0.0 °C | |
| Symbol |
GHS02 |
Signal Word | Warning | |
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A highly enantioselective phosphabicyclooctane catalyst for the kinetic resolution of benzylic alcohols.
J. Am. Chem. Soc. 125(14) , 4166-73, (2003) A new class of chiral phosphines belonging to the P-aryl-2-phosphabicyclo[3.3.0]octane family (PBO) has been prepared by enantioselective synthesis starting from lactate esters and 2,2-dimethylcyclopentanone enolate 5. A selective enolate alkylation method ha... |
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Synthesis of novel C-2 substituted vitamin D derivatives having ringed side chains and their biological evaluation on bone.
J. Steroid Biochem. Mol. Biol. 136 , 3-8, (2013) Up to the present, numerous vitamin D derivatives have been synthesized, but most of them have straight side chains, and there are few publications described about in vitro and in vivo evaluations on bone by vitamin D derivatives. In our previous paper, we re... |
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Synthesis of the spirosuccinimide moiety of Asperparaline A.
Biosci. Biotechnol. Biochem. 64(8) , 1758-60, (2000) 2,6,6-Trimethyl-2-azaspiro[4.4]nonane-1,3-dione (9), a spirosuccinimide moiety of asperparaline A (1), was synthesized by starting from 2,2-dimethylcyclopentanone (4) via trinitrile 6 in five steps in a moderate yield. This conversion establishes a model stud... |
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Regioselective Synthesis of 2, 2-Dimethylcyclopentanone Using 2-Pyrrolidone Magnesium Salt as Electrogenerated Base. Bonafoux D, et al.
Synth. Commun. 28(1) , 93-98, (1998)
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Synthesis of pyrrolizidine oximes 222 and 236: Novel alkaloids of a dendrobatid poison frog. Rutchinson KD, et al.
Tetrahedron 50(21) , 6129-36, (1994)
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Synthesis of catalpalactone. Lane KJ and Pinder AR.
J. Org. Chem. 47(16) , 3171-72, (1982)
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