67323-96-0 Usage
Uses
Used in Flavor and Fragrance Industry:
(E)-4-ETHOXY-NONA-1,5-DIENE is used as a key ingredient in the flavor and fragrance industry, particularly for the production of perfumes, soaps, and other personal care products. Its sweet, floral odor makes it a valuable addition to these products, enhancing their overall scent and appeal.
Used in Organic Synthesis:
In the field of organic synthesis, (E)-4-ETHOXY-NONA-1,5-DIENE serves as a crucial precursor. Its unique molecular structure allows for further chemical reactions and modifications, leading to the creation of a wide range of compounds with various applications.
Used in Pharmaceutical Production:
(E)-4-ETHOXY-NONA-1,5-DIENE is also utilized in the production of pharmaceuticals. Its properties make it a valuable component in the development of new drugs, potentially contributing to advancements in medicine and healthcare.
Used in the Food Industry:
As a flavoring agent, (E)-4-ETHOXY-NONA-1,5-DIENE is employed in the food industry to enhance the taste and aroma of various products. Its sweet, floral scent can add a pleasant and distinctive flavor to a range of food items, making it a sought-after ingredient in the culinary world.
Check Digit Verification of cas no
The CAS Registry Mumber 67323-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,2 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67323-96:
(7*6)+(6*7)+(5*3)+(4*2)+(3*3)+(2*9)+(1*6)=140
140 % 10 = 0
So 67323-96-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-4-7-8-10-11(9-5-2)12-6-3/h5,8,10-11H,2,4,6-7,9H2,1,3H3/b10-8+
67323-96-0Relevant academic research and scientific papers
Anzalone, Peter W.,Baru, Ashvin R.,Danielson, Eric M.,Hayes, Patrick D.,Nguyen, Mai P.,Panico, Ambrose F.,Smith, Russell C.,Mohan, Ram S.
, p. 2091 - 2096 (2005)
(Chemical Equation Presented) Three one-pot methods for the conversion of aldehydes to homoallyl ethers catalyzed by Bi(OTf)3? xH 2O (1 x 4) have been developed. The one-pot synthesis of homoallyl ethers can be achieved either by