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(E,E)-6-methyl-8-(benzyloxy)-2,6-octadien-1-ol, an organic compound with the molecular formula C15H20O2, is a member of the octadien-1-ol group. This colorless to pale yellow liquid exhibits a floral, green, and sweet odor, making it a valuable component in the creation of perfumes and fragrances. Beyond its aromatic applications, it also serves as a building block in the synthesis of pharmaceuticals and contributes to the flavor profile in the food industry. Furthermore, research has explored its potential as an antioxidant and antitumor agent.

100571-29-7

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100571-29-7 Usage

Uses

Used in Perfumery and Fragrance Industry:
(E,E)-6-methyl-8-(benzyloxy)-2,6-octadien-1-ol is used as a key ingredient in the perfumery and fragrance industry for its floral, green, and sweet scent, enhancing the overall aroma of various products.
Used in Pharmaceutical Synthesis:
This chemical compound is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications.
Used in the Food Industry:
(E,E)-6-methyl-8-(benzyloxy)-2,6-octadien-1-ol is employed as a flavoring agent in the food industry, adding a unique taste and aroma to different products.
Used in Antioxidant and Antitumor Research:
(E,E)-6-methyl-8-(benzyloxy)-2,6-octadien-1-ol is used as a subject of study in the fields of antioxidant and antitumor research, with the aim of discovering its potential benefits in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 100571-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,7 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100571-29:
(8*1)+(7*0)+(6*0)+(5*5)+(4*7)+(3*1)+(2*2)+(1*9)=77
77 % 10 = 7
So 100571-29-7 is a valid CAS Registry Number.

100571-29-7Relevant academic research and scientific papers

Studies on taxadiene synthase: interception of the cyclization cascade at the verticillene stage and rearrangement to phomactatriene

Chow, Siew Yin,Williams, Howard J.,Pennington, James D.,Nanda, Samik,Reibenspies, Joseph H.,Scott, A. Ian

, p. 6204 - 6209 (2008/02/05)

The cyclization of geranylgeranyl diphosphate (GGDP) to taxadiene catalyzed by taxadiene synthase has been suggested to proceed in stages, involving a transient bicyclic verticillyl carbocation intermediate, which also has been proposed in the biosyntheti

The Synthesis of Cembranolide Precursors via Addition of Allylstannanes to Conjugated Aldehydes

Marshall, James A.,DeHoff, Bradley S.

, p. 863 - 872 (2007/10/02)

The Lewis acid promoted addition of functionalized allylstannanes A9, C10, and C11 to a variety of conjugated aldehydes was examined as a possible route to acyclic precursors of macrocyclic diterpenoids.Additions to crotonaldehyde proceeded as expected, g

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