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TRIMETHYL-1,5,9-CYCLODODECATRIENE, with the molecular formula C15H26, is a chemical compound characterized by its clear, colorless liquid form and a distinctive fruity aroma. It is a versatile building block in the synthesis of aromatic compounds, owing to its unique molecular structure.

21064-19-7

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21064-19-7 Usage

Uses

Used in Flavor and Fragrance Industry:
TRIMETHYL-1,5,9-CYCLODODECATRIENE is utilized as a key ingredient in the production of flavors and fragrances due to its natural presence in essential oils and its ability to contribute to the creation of a wide array of aromatic compounds.
Used in Perfumery:
In the perfumery industry, TRIMETHYL-1,5,9-CYCLODODECATRIENE serves as a raw material for synthesizing perfumes, enhancing their scent profiles and providing a fruity note to the final product.
Used in Food Industry:
As a component in food flavorings, TRIMETHYL-1,5,9-CYCLODODECATRIENE is used to impart specific taste and aroma characteristics to various food products, capitalizing on its natural and appealing scent.
Used in Plastics and Polymers Industry:
TRIMETHYL-1,5,9-CYCLODODECATRIENE also functions as a chemical intermediate in the manufacturing process of plastics and polymers, contributing to the development of new materials with specific properties.
Safety Note:
It is important to handle TRIMETHYL-1,5,9-CYCLODODECATRIENE with caution due to its flammable nature and potential to cause skin and eye irritation upon contact. Proper safety measures should be implemented during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21064-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,6 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21064-19:
(7*2)+(6*1)+(5*0)+(4*6)+(3*4)+(2*1)+(1*9)=67
67 % 10 = 7
So 21064-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-13-7-4-9-14(2)11-6-12-15(3)10-5-8-13/h7,10-11H,4-6,8-9,12H2,1-3H3/b13-7+,14-11+,15-10+

21064-19-7Upstream product

21064-19-7Relevant academic research and scientific papers

Using Terpene Synthase Plasticity in Catalysis: On the Enzymatic Conversion of Synthetic Farnesyl Diphosphate Analogues

Hou, Anwei,Dickschat, Jeroen S.

supporting information, p. 15644 - 15649 (2021/10/04)

Four synthetic farnesyl diphosphate analogues were enzymatically converted with three bacterial sesquiterpene synthases, including β-himachalene synthase (HcS) and (Z)-γ-bisabolene synthase (BbS) from Cryptosporangium arvum, and germacrene A synthase (SmTS6) from Streptomyces mobaraensis. These enzyme reactions not only yielded several previously unknown compounds, showing that this approach opened the door to a new chemical space, but substrates with blocked or altered reactivities also gave interesting insights into the cyclisation mechanisms and the potential to catalyse reactions with different initial cyclisation modes.

METHOD FOR PRODUCING TRIMETHYLCYCLODODECATRIENE

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Page/Page column 9-10, (2008/06/13)

The invention relates to the production of trimethylcyclododecatriene in a continuous or discontinuous method, by the trimerisation of isoprene in the presence of a catalyst system and a solvent. The raw trimethylcyclododecatriene obtained can be isolated by distillation. The dimethylcyclooctadiene formed as a by-product can also be isolated from the raw product.

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