40267-53-6 Usage
Description
(E)-N,N-Diethyl-3,7-dimethyl-2,6-octadiene-1-amine, commonly known as octodiene, is a chemical compound with the molecular formula C14H29N. It is a tertiary amine characterized by its floral, fruity, and slightly green odor. Octodiene is a clear, colorless liquid that is soluble in alcohol and oils, making it versatile for use in a variety of applications. It is commonly used as a fragrance ingredient in perfumes and colognes, as well as a flavoring agent in the food industry. Additionally, it serves as a chemical intermediate in the synthesis of other compounds. However, it should be handled with care due to its potential to cause skin and eye irritation.
Uses
Used in Fragrance Industry:
Octodiene is used as a fragrance ingredient for its pleasant, floral, fruity, and slightly green scent. It is added to perfumes and colognes to enhance their overall aroma and appeal to consumers.
Used in Cosmetic and Personal Care Products:
In the cosmetic and personal care industry, octodiene is utilized for its agreeable scent, often added to products to provide a more enjoyable user experience.
Used in Flavoring Industry:
As a flavoring agent, octodiene contributes to the taste and aroma of various food products, enhancing their overall flavor profile and consumer appeal.
Used as a Chemical Intermediate:
Octodiene also serves as a chemical intermediate in the synthesis of other compounds, playing a crucial role in the production of various chemical products.
Please note that the provided materials do not mention any specific applications of octodiene in drug delivery systems or anticancer applications. The information given focuses on its use in the fragrance, cosmetic, personal care, and flavoring industries, as well as its role as a chemical intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 40267-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,6 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40267-53:
(7*4)+(6*0)+(5*2)+(4*6)+(3*7)+(2*5)+(1*3)=96
96 % 10 = 6
So 40267-53-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H27N/c1-6-15(7-2)12-11-14(5)10-8-9-13(3)4/h9,11H,6-8,10,12H2,1-5H3/b14-11+
40267-53-6Relevant articles and documents
Rhodium-Catalyzed Asymmetric Synthesis of β-Branched Amides
Wu, Zhao,Laffoon, Joshua D.,Nguyen, Trang T.,McAlpin, Jacob D.,Hull, Kami L.
supporting information, p. 1371 - 1375 (2017/01/24)
A general asymmetric route for the one-step synthesis of chiral β-branched amides is reported through the highly enantioselective isomerization of allylamines, followed by enamine exchange, and subsequent oxidation. The enamine exchange allows for a rapid and modular synthesis of various amides, including challenging β-diaryl and β-cyclic.
Copper(II) catalyzed allylic amination of terpenic chlorides in water
Boualy, Brahim,Harrad, Mohamed Anouar,El Houssame, Soufiane,El Firdoussi, Larbi,Ali, Mustapha Ait,Karim, Abdallah
experimental part, p. 46 - 50 (2012/04/10)
A highly efficient method for the synthesis of allylic amines from terpenic chlorides by cheap copper (II) as catalyst in water has been developed. Allylic chlorides react with high regioselectivity in the presence of secondary amines, under mild conditions to give N-allylic amines in excellent yields.
Process for producing optically active 3, 7-dimethyl-6-octenol and process for producing intermediate therefor
-
, (2008/06/13)
Provided is citronellol, which has an elegant rosy fragrance and is extremely useful for fragrance impartation to aromatic articles. A mixture of an alkylamine and isoprene in a molar ratio of from 1:4 to 1:4.5 is subjected to telomerization at 80 to 100° C. for 2.5 to 3.5 hours in the presence of an alkyllithium catalyst and/or phenyllithium catalyst to obtain a nerylamine compound containing 2 to 10 wt % α-nerylamine compound represented by general formula (4). From this nerylamine compound, citronellol containing 2 to 10 wt % optically active 3,7-dimethyl-7-octenol is produced through the reaction steps of asymmetric isomerization, hydrolysis, and hydrogenation.
