General description
2-Adamantanone on deprotonation in the gas phase affords the corresponding β-enolate anion. It reacts with 1,1-dilithio-1-sila-2,3,4,5-tetraphenylsilole to yield 5-silafulvene.
Application
2-Adamantanone was used in the synthesis of dispiro N-Boc-protected 1,2,4-trioxane and (+/-)-1-(adamantan-2-yl)-2-propanamine.
Legal Information
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Molecular Weight: 150.22. Empirical Formula: C10H14O. Quality Level: 100. product line: ReagentPlus®. . Assay: 99%. form: solid. mp: 256-258 . °C (subl.) (lit.). SMILES string: O: C1C2CC3CC(C2)CC1C3. InChI: 1S/C10H14O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-9H,1-5H2/t6-,7+,8-,9+. InChI key: IYKFYARMMIESOX-SPJNRGJMSA-N. Storage Class Code: 11 - Combustible Solids. WGK: WGK 2. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves.- UPC:
- 12141736
- Condition:
- New
- HazmatClass:
- No
- MPN:
- 146048-25G
- CAS:
- 700-58-3
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