13380-94-4 Usage
Description
TRICYCLO[5.2.1.02,6]DECAN-8-ONE is a complex organic compound with a unique cyclic structure. It is characterized by its tricyclic framework and a ketone functional group, which contributes to its chemical properties and potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
TRICYCLO[5.2.1.02,6]DECAN-8-ONE is used as a synthetic intermediate for the development of novel pharmaceutical compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
TRICYCLO[5.2.1.02,6]DECAN-8-ONE serves as a reagent in the synthesis of various organic compounds, including hindered olefins and other complex molecules. Its versatility in chemical reactions makes it a valuable component in the development of new materials and substances.
Used in Polymer Industry:
TRICYCLO[5.2.1.02,6]DECAN-8-ONE is used as a reagent to enhance the glass transition temperature of polymethyl methacrylate (PMMA). By increasing the temperature at which the polymer transitions from a hard, glassy state to a rubbery state, it can improve the material's overall performance and durability.
Safety Profile
Moderately toxic by ingestion and skin contact. When heated to decomposition it emits acrid smoke and irritating fumes.
Check Digit Verification of cas no
The CAS Registry Mumber 13380-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,8 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13380-94:
(7*1)+(6*3)+(5*3)+(4*8)+(3*0)+(2*9)+(1*4)=94
94 % 10 = 4
So 13380-94-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O/c11-10-5-6-4-9(10)8-3-1-2-7(6)8/h6-9H,1-5H2/t6-,7-,8-,9-/m1/s1
13380-94-4Relevant articles and documents
The thermal runaway of a hydrogen-transfer reaction
West, Andrew V.,Newman, Chris P.
, p. 304 - 307 (2002)
A thermal runaway is reported which occurred during the conversion of an unsaturated alcohol to the saturated ketone via internal hydrogen transfer. An unexpected and extremely rapid rise in temperature and pressure was observed when the reaction was run
Method of making carbonyl compounds
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Page/Page column 3-4, (2008/06/13)
A method of making a carbonyl compound comprises contacting a compound comprising a secondary hydroxyl group with a basic metal oxide catalyst at a temperature sufficient to maintain the compound comprising a secondary hydroxyl group in a vapor phase.
PREPARATION OF KETONE CONTAINING CYCLIC COMPOUNDS
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Page/Page column 3-4, (2008/06/13)
A method of preparing a polycyclic compound containing a ketone functionality comprising: reacting a mixture comprising a catalyst, a reactant compound and an amount of water greater than or equal to 3 weight percent (wt %) based on the weight of the reactant compound; wherein said catalyst comprises nickel and base and said reactant compound comprises at least two fused rings, A and B wherein ring A is a saturated ring or ring system having 5 to 7 cyclic carbons and substituted with a hydroxyl functionality and ring B is a non-aromatic unsaturated ring having 5 to 6 cyclic carbons; and converting the hydroxyl functionality of ring A to a ketone functionality and non-aromatic unsaturated ring B to a saturated ring.
