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10,11-epoxy-3,7,11-trimethyl-2,6-dodecadien-1-ol acetate, also known as jasmolactone, is a complex organic compound with the molecular formula C16H28O3. It is a colorless to pale yellow liquid with a strong, sweet, floral odor. This chemical is derived from jasmine oil and is used as a fragrance ingredient in various applications, including perfumes, cosmetics, and household products. Jasmolactone is synthesized through a series of chemical reactions involving the epoxidation of 3,7,11-trimethyl-2,6-dodecadien-1-ol, followed by the acetylation of the resulting epoxy alcohol. Due to its unique scent profile, it is often used to mimic the aroma of natural jasmine in commercial products.

29442-57-7

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29442-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29442-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 29442-57:
(7*2)+(6*9)+(5*4)+(4*4)+(3*2)+(2*5)+(1*7)=127
127 % 10 = 7
So 29442-57-7 is a valid CAS Registry Number.

29442-57-7Relevant academic research and scientific papers

Exploiting the Potential of Meroterpenoid Cyclases to Expand the Chemical Space of Fungal Meroterpenoids

Abe, Ikuro,Barra, Lena,Cheng, Andrea,Fujita, Makoto,Kikuchi, Takashi,Kojasoy, Volga,Mitsuhashi, Takaaki,Porco, John A.,Powers, Zachary,Taniguchi, Yoshimasa,Tantillo, Dean J.,Yang, Feng

, p. 23772 - 23781 (2020/10/23)

Fungal meroterpenoids are a diverse group of hybrid natural products with impressive structural complexity and high potential as drug candidates. In this work, we evaluate the promiscuity of the early structure diversity-generating step in fungal meroterpenoid biosynthetic pathways: the multibond-forming polyene cyclizations catalyzed by the yet poorly understood family of fungal meroterpenoid cyclases. In total, 12 unnatural meroterpenoids were accessed chemoenzymatically using synthetic substrates. Their complex structures were determined by 2D NMR studies as well as crystalline-sponge-based X-ray diffraction analyses. The results obtained revealed a high degree of enzyme promiscuity and experimental results which together with quantum chemical calculations provided a deeper insight into the catalytic activity of this new family of non-canonical, terpene cyclases. The knowledge obtained paves the way to design and engineer artificial pathways towards second generation meroterpenoids with valuable bioactivities based on combinatorial biosynthetic strategies.

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