54878-25-0

Basic information

• Product Name: (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one
• Synonyms: (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one
• CAS NO: 54878-25-0
• Molecular Formula: C₁₅H₂₂O
• Molecular Weight: 218.33
• Mol File: 54878-25-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 321.4°C at 760 mmHg
• Flash Point: 143.2°C
• Appearance: /
• Density: 0.96g/cm³
• Vapor Pressure: 0.0003mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one(54878-25-0)
• EPA Substance Registry System: (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one(54878-25-0)

Safety Data

• Hazardous Substances Data: 54878-25-0(Hazardous Substances Data)

Usage

Description

(2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one is a cyclic ketone derived from spiro[4.5]dec-6-en-8-one, with hydrogens at positions 6 and 10 substituted by methyl groups, and an isopropenyl group at position 2, specifically in the (2R,5S,10R)-diastereoisomeric form.

Uses

Used in Pharmaceutical Industry:
(2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one is used as a potential pharmaceutical compound for its unique structural properties and potential interactions with biological targets. Its cyclic ketone structure and specific substitutions may allow it to modulate various biological pathways, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one can be used as a starting material or a building block for the synthesis of more complex molecules with specific biological activities. Its unique structure may provide insights into the design and development of novel compounds with tailored properties for various applications.
Used in Material Science:
The unique structural features of (2R,6R)-6,10-dimethyl-2-prop-1-en-2-yl-spiro[4.5]dec-9-en-8-one may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.

InChI:InChI=1/C15H22O/c1-10(2)13-5-6-15(9-13)11(3)7-14(16)8-12(15)4/h7,12-13H,1,5-6,8-9H2,2-4H3/t12-,13-,15?/m1/s1

Upstream product

• 79265-79-5 (2S^*,5S^*,10R^*)-2-hydroxy-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-78-4 (2R^*,5R^*,10S^*)-2-hydroxy-6,10-dimethylspiro<4.5>dec-6-en-8-one 
• 79276-44-1 (2S^*,5S^*,10R^*)-2-mesyloxy-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-80-8 (2R^*,5S^*,10R^*)-2-bis(ethoxycarbonyl)methyl-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-81-9 2-((8S,10R,13R)-7,13-Dimethyl-1,4-dithia-dispiro[4.2.4.2]tetradec-6-en-10-yl)-malonic acid monoethyl ester 
• 79265-82-0 (2R^*,5S^*,10R^*)-2-(1-ethoxycarbonylvinyl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-83-1 (2R^*,5S^*,10R^*)-2-(3-hydroxypropen-2-yl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 79265-84-2 (2R^*,5S^*,10R^*)-2-(3-chloropropen-2-yl)-6,10-dimethylspiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 73879-10-4 4-(2,2-ethylenedioxyethyl)-3,5-dimethyl-3,6-dihydroanisole 
• 79265-85-3 (2R^*,5S^*,10R^*)-6,10-dimethyl-2-(2-propenyl)spiro<4.5>dec-6-en-8-one ethylene dithioacetal 
• 34181-46-9 11-hydroxysolavetivone 
• 137895-82-0 (-)-(5S,6R,9R)-9-isopropenyl-6-methyl-5-(trimethylsilyl)bicyclo<4.4.0>dec-1-en-3-one 3-ethylene thioacetal 
• 137895-81-9 (-)-(5S,6R,9R)-9-isopropenyl-6-methyl-5-(trimethylsilyl)bicyclo<4.4.0>dec-1-en-3-one 
• 137895-84-2 (-)-(1R,2S,5S,6R,8R)-5,6-epoxy-8-isopropenyl-1-methyl-2-(trimethylsilyl)bicyclo<4.4.0>decane 

Downstream Products

• 35951-50-9 (+)-lubimin 
• 103573-06-4 oxysolavetivone 

Relevant articles and documents

Total synthesis of (-)-solavetivone using enantioselective copper-catalysed conjugate addition of Me3Al to a cyclohexa-2,5-dienone intermediate

By applying a new enantioselective Cu-catalysed conjugate addition of Me3Al, (-)-solavetivone 1 is synthesized stereoselectively from cyclohexa-2,5-dienone 4, prepared from a chiral compound 6 using a regioselective HgII-mediated cyc

Total synthesis of (±)-solavetivone and aglycone A3. Regio- and stereo-selective birch reduction of 6,10-dimethyl-2-hydroxy-spiro[4,5]deca-6,9-dien-8-one

-