About This Item
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Assay
98%
form
solid
mp
>300 °C (lit.)
functional group
hydroxyl
ketone
SMILES string
O[C@]12C[C@@H]3C[C@H](C1)C(=O)[C@@H](C3)C2
InChI
1S/C10H14O2/c11-9-7-1-6-2-8(9)5-10(12,3-6)4-7/h6-8,12H,1-5H2/t6-,7-,8+,10-
InChI key
TZBDEVBNMSLVKT-XYYXLIQBSA-N
General description
Application
- As a model compound to investigate the application of lanthanide NMR shift reagents for the analysis of disubstituted derivative of adamantane.[1]
- As a starting material for the synthesis of E-2-amino-5-hydroxyadamantane.[3]
- As a starting material for the synthesis of 4-(triphenylsilyloxy)adamantan-1-ol.[4]
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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