53771-60-1 Usage
Uses
Used in the Food and Beverage Industry:
(E)-3,7-dimethyl-octa-1,5,7-trien-3-yl acetate is used as a flavoring agent for its fruity and floral aroma, enhancing the taste and scent of various products in this industry.
Used in Perfumes and Fragrances:
In the perfumery and fragrance industry, (E)-3,7-dimethyl-octa-1,5,7-trien-3-yl acetate is used as a key ingredient for its appealing scent, contributing to the creation of complex and long-lasting fragrances.
Used in the Production of Essential Oils:
(E)-3,7-dimethyl-octa-1,5,7-trien-3-yl acetate is also utilized in the production of essential oils, where its distinct aroma plays a significant role in the overall composition and quality of the final product.
Used in Tobacco Products:
(E)-3,7-dimethyl-octa-1,5,7-trien-3-yl acetate is employed as a flavoring agent in the tobacco industry, adding a pleasant aroma to tobacco products.
Used in Pharmaceutical Research:
(E)-3,7-dimethyl-octa-1,5,7-trien-3-yl acetate has been studied for its potential medicinal properties, including anti-inflammatory and antioxidant effects, indicating its use as a subject of research in the pharmaceutical industry for possible therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 53771-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,7 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53771-60:
(7*5)+(6*3)+(5*7)+(4*7)+(3*1)+(2*6)+(1*0)=131
131 % 10 = 1
So 53771-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c1-6-12(5,14-11(4)13)9-7-8-10(2)3/h6-8H,1-2,9H2,3-5H3/b8-7+
53771-60-1Relevant academic research and scientific papers
A practical and convenient synthesis of hotrienol, an excellent fruity smelling compound
Yuasa, Yoshifumi,Kato, Yasushi
, p. 4036 - 4039 (2007/10/03)
The practical and convenient synthesis of hotrienol, which is an excellent fruity smelling compound, has been performed by the ene-type chlorination of linalyl acetate and then dehydrochlorinated by lithium bromide and lithium carbonate in DMF, followed by hydrolysis in three steps with an overall yield of 55%.
