69925-33-3 Usage
Uses
Used in Flavor and Fragrance Industry:
4,7-Octadienoic acid, ethyl ester, (Z)is used as a flavoring agent for its fresh, fruity, and pineapple-like aroma. It is commonly employed in the development of food products, beverages, and confectionery items to impart a tropical and refreshing taste.
Used in Perfumery:
In the perfumery industry, 4,7-Octadienoic acid, ethyl ester, (Z)is used as a fragrance ingredient to create a natural and pleasant scent. Its unique top note and fruity character make it suitable for use in various perfumes, colognes, and other scented products.
Used in Aromatherapy:
4,7-Octadienoic acid, ethyl ester, (Z)can also be used in aromatherapy for its uplifting and invigorating properties. Its fresh and fruity aroma can help to create a sense of relaxation and well-being, making it a popular choice for use in essential oils and aromatherapy blends.
Used in Cosmetics and Personal Care Products:
Due to its pleasant and natural scent, 4,7-Octadienoic acid, ethyl ester, (Z)is used in the formulation of cosmetics and personal care products such as lotions, creams, and body washes. It adds a refreshing and tropical fragrance to these products, enhancing the overall sensory experience for the user.
Check Digit Verification of cas no
The CAS Registry Mumber 69925-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,2 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69925-33:
(7*6)+(6*9)+(5*9)+(4*2)+(3*5)+(2*3)+(1*3)=173
173 % 10 = 3
So 69925-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-3-5-6-7-8-9-10(11)12-4-2/h3,6-7H,1,4-5,8-9H2,2H3/b7-6-
69925-33-3Relevant academic research and scientific papers
Synthesis of Ethyl (Z)-4,7-Octadienoate
Vig, O. P.,Sharma, M. L.,Bhanot, R. K.,Malik, Neera
, p. 970 - 971 (2007/10/02)
Alkylation of the dianion of propargyl alcohol with allyl bromide provides hex-2-yn-5-en-1-ol (II) which on catalytic hydrogenation with Lindlar's catalyst yields (Z)-2,5-hexadien-1-ol (III).Conversion of III into the bromide (IV) and subsequent alkylation of monosodiomalonate with IV in benzene/DMF mixture furnishes the diester (V).Half-hydrolysis of V gives the acid ester (VI) which on decarboxylation with HMPA affords ethyl (Z)-4,7-octadienoate (I).
