28980-74-7 Usage
Uses
Used in Fragrance and Flavoring Industry:
2-methyldodeca-3,5-diene is used as a key ingredient in the production of fragrances and flavorings for its characteristic odor. It contributes to the creation of a wide range of scents and tastes in various consumer products, including perfumes, cosmetics, and food items.
Used in Organic Synthesis:
2-methyldodeca-3,5-diene is utilized as an intermediate in the synthesis of various organic compounds. Its unique structure with two double bonds allows for a variety of chemical reactions, making it a versatile building block in the development of new molecules and materials.
Used in Research and Development:
Due to its chemical properties and reactivity, 2-methyldodeca-3,5-diene is employed in research and development settings to explore new chemical reactions, pathways, and applications. It serves as a valuable tool for scientists and researchers in the field of organic chemistry to advance their understanding of chemical processes and develop innovative solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 28980-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28980-74:
(7*2)+(6*8)+(5*9)+(4*8)+(3*0)+(2*7)+(1*4)=157
157 % 10 = 7
So 28980-74-7 is a valid CAS Registry Number.
28980-74-7Relevant academic research and scientific papers
Mechanistic Aspects and Profiles of the Double Elimination Reaction of β-Substituted Sulfones
Otera, Junzo,Misawa, Hiromitsu,Sugimoto, Kiyoto
, p. 3830 - 3833 (2007/10/02)
The double elimination reaction of β-acetoxy or β-alkoxy sulfones was investigated in detail by employing some representative reactions.Successful isolation of reaction intermediates revealed the reaction path: the first step is elimination of the acetoxy group to afford a vinyl sulfone.The subsequent elimination of a phenylsulfonyl group from the vinyl sulfone gives acetylenes, while polyenes are formed in cases where isomerization of the vinyl sulfone to an allyl sulfone is possible prior to the second elimination.Besides these mechanistic considerations, general features are discussed in order to make clear the scope and limitations of this synthetically useful reaction.
