2549-61-3

Usage

Uses

Used in Chemical Synthesis:
ALPHA-METHYL-EPSILON-CAPROLACTONE is used as a synthetic building block for the production of various chemicals and pharmaceuticals. Its unique structure allows for the creation of a wide range of compounds with diverse applications.
Used in Pharmaceutical Industry:
ALPHA-METHYL-EPSILON-CAPROLACTONE is used as an intermediate in the synthesis of pharmaceutical compounds. Its ability to be modified and incorporated into complex molecules makes it a valuable asset in the development of new drugs.
Used in Polymer Industry:
ALPHA-METHYL-EPSILON-CAPROLACTONE is used as a monomer in the production of biodegradable polymers. Its unique properties contribute to the development of environmentally friendly materials with potential applications in packaging, agriculture, and medical devices.
Used in Flavor and Fragrance Industry:
ALPHA-METHYL-EPSILON-CAPROLACTONE is used as a component in the creation of various flavors and fragrances. Its distinct chemical properties allow for the development of unique scents and tastes that can be used in the food, beverage, and cosmetic industries.
Used in Research and Development:
ALPHA-METHYL-EPSILON-CAPROLACTONE is used as a research compound for studying its properties and potential applications. Its unique structure and reactivity make it an interesting subject for scientific investigation, which could lead to the discovery of new uses and applications in various fields.

InChI:InChI=1/C7H12O2/c1-6-4-2-3-5-9-7(6)8/h6H,2-5H2,1H3

Downstream Products

• 137305-44-3 (E)-5-Methyl-6-oxo-8-phenylsulfanyl-oct-7-enal 
• 137305-54-5 methyl (+/-)-(3aR*,4S*,5S*,7aS*)-3a,4,5,6,7,7a-hexahydro-7a-methyl-7-oxo-5-phenylthioindane-4-carboxylate 
• 137305-50-1 methyl (+/-)-(3aR*,4S*,5S*,7aS*)-7-(tert-butyldimethylsiloxy)-3a,4,5,7a-tetrahydro-7a-methyl-5-phenylthioindane-4-carboxylate 
• 137305-53-4 methyl (2Z,9Z)-7-methyl-8-oxo-10-(phenylthio)deca-2,9-dienoate 
• 137305-46-5 methyl (2E,9Z)-7-methyl-8-oxo-10-(phenylthio)deca-2,9-dienoate 
• 137305-52-3 methyl (2Z,9E)-7-methyl-8-oxo-10-(phenylthio)deca-2,9-dienoate 
• 137305-45-4 methyl (2E,9E)-7-methyl-8-oxo-10-(phenylthio)deca-2,9-dienoate 
• 144880-24-0 (E)-8-(4-Methoxy-phenylsulfanyl)-5-methyl-6-oxo-oct-7-enal 
• 144880-48-8 methyl (E,E)-7-methyl-8-oxo-10-phenylsulfinyldeca-2,9-dienoate 
• 137305-54-5 methyl (+/-)-(3aR*,4S*,5R*,7aR*)-3a,4,5,6,7,7a-hexahydro-7a-methyl-7-oxo-5-phenylthioindane-4-carboxylate 
• 144880-28-4 methyl (2E,9Z)-10-(4-methoxyphenylthio)-7-methyl-8-oxodeca-2,9-dienoate 
• 144880-26-2 methyl (2E,9E)-10-(4-methoxyphenylthio)-7-methyl-8-oxodeca-2,9-dienoate 
• 144880-36-4 methyl (+/-)-(3aR*,4S*,5S*,7aS*)-3a,4,5,6,7,7a-hexahydro-5-(4-methoxyphenylthio)-7a-methyl-7-oxoindane-4-carboxylate 
• 144880-36-4 methyl (+/-)-(3aR*,4S*,5R*,7aR*)-3a,4,5,6,7,7a-hexahydro-5-(4-methoxyphenylthio)-7a-methyl-7-oxoindane-4-carboxylate 

Relevant academic research and scientific papers

Novel photolactonisation from xanthenoic esters

In the context of our work on photocleavable fragrance precursors, we have discovered a new photo-fragmentation of xanthenoic esters into xanthene- and formyl radicals. This homolytic cleavage has not been reported previously. Thus, unsaturated formyl radicals cyclise to lactones of various ring size.