79604-66-3 Usage
Uses
Used in Flavoring and Fragrance Industry:
2,4,6-Trimethyl-1,6-heptadien-4-ol is utilized as a flavoring and fragrance agent, adding distinctive scents and tastes to food products and cosmetics. Its strong odor makes it a valuable component in creating appealing sensory experiences for consumers.
Used in Chemical Synthesis:
2,4,6-Trimethyl-1,6-heptadien-4-ol serves as an intermediate in the synthesis of various organic compounds, contributing to the development of a wide range of chemical products and materials.
Used in Antimicrobial Applications:
2,4,6-Trimethyl-1,6-heptadien-4-ol has been studied for its potential antimicrobial properties, suggesting its use in applications where inhibiting the growth of microorganisms is necessary, such as in preservatives or sanitizing agents.
Used in Antioxidant Applications:
Its antioxidant potential indicates that 2,4,6-Trimethyl-1,6-heptadien-4-ol could be employed in formulations designed to prevent oxidation in various products, thereby extending their shelf life or protecting them from degradation.
It is crucial to handle 2,4,6-Trimethyl-1,6-heptadien-4-ol with care due to its potential to cause irritation to the skin, eyes, and respiratory system, emphasizing the need for proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 79604-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79604-66:
(7*7)+(6*9)+(5*6)+(4*0)+(3*4)+(2*6)+(1*6)=163
163 % 10 = 3
So 79604-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-8(2)6-10(5,11)7-9(3)4/h11H,1,3,6-7H2,2,4-5H3
79604-66-3Relevant academic research and scientific papers
Highly diastereoselective intramolecular allylation reactions of mixed silyl-substituted acetals
Linderman, Russell J.,Chen, Kangyi
, p. 2441 - 2453 (2007/10/03)
The reaction of preformed mixed acetals derived from (α-hydroxyalkyl)dimethylallylsilane with a number of aromatic and aliphatic aldehydes in the presence of Lewis acids results in a highly diastereoselective intramolecular allylation reaction. The reaction proceeds through a cyclic synclinal SE′ addition of the allylsilane to an intermediate oxocarbenium ion. The reaction occurs exclusively by an intramolecular process as determined by means of a cross-over experiment. The relative stereochemistry was determined by the conversion of one of the allylation products to a known (stereodefined) aldol-type product. A greater degree of diastereoselectivity is obtained by in-situ formation of an oxocarbenium ion from (α-hydroxyhexyl)dimethylallylsilane and an aldehyde in the presence of boron trifluoride etherate. The diastereoselectivity of the in-situ allylation reaction typically exceeds 100:1 in favor of the syn adduct. However, reactions with electron rich aryl aldehydes resulted in a diminished degree of diastereoselectivity. The initial product of the in-situ reaction is an unstable silyl fluoride which is readily hydrolyzed to a silanol derivative upon reaction with methanolic potassium hydroxide. The overall yield of the two-step process is greater than 80%. A method for the synthesis of more highly substituted (α-alkoxyalkyl)dimethylallylsilanes by allyl anion displacement of methoxide from silicon is also described. The methyl siloxane derivatives were obtained by ozonolytic cleavage of an unsubstituted allyl group in methanol.
