66410-24-0 Usage
Description
(3Z,13Z)-3,13-Octadecadien-1-ol, also known as linoleic acid, is a polyunsaturated omega-6 fatty acid with a conjugated double bond system. It is an essential nutrient that plays a crucial role in various biological processes and has been extensively studied for its potential health benefits.
Uses
Used in Pharmaceutical Industry:
(3Z,13Z)-3,13-Octadecadien-1-ol is used as a pharmaceutical agent for its potential therapeutic effects on various health conditions. It has been shown to have anti-inflammatory, anti-atherogenic, and anti-cancer properties, making it a valuable compound for the development of new drugs and treatments.
Used in Nutritional Supplements:
As an essential fatty acid, (3Z,13Z)-3,13-Octadecadien-1-ol is used in the formulation of nutritional supplements to support overall health and well-being. It is particularly important for maintaining healthy skin, hair, and nails, as well as for promoting heart and brain health.
Used in Cosmetics Industry:
(3Z,13Z)-3,13-Octadecadien-1-ol is used as an ingredient in the cosmetics industry due to its moisturizing and anti-inflammatory properties. It is often found in skincare products, such as creams and lotions, to help improve skin hydration and reduce the appearance of fine lines and wrinkles.
Used in Food Industry:
In the food industry, (3Z,13Z)-3,13-Octadecadien-1-ol is used as an additive to enhance the nutritional value of various products. It is often found in vegetable oils, margarine, and other processed foods as a source of essential fatty acids.
Used in Biomedical Research:
(3Z,13Z)-3,13-Octadecadien-1-ol is used in biomedical research for the study of the compositional and antioxidant properties of oils and extracts from various sources, such as Diarthron vesiculosum. This research can help to better understand the potential health benefits and applications of this compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 66410-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,1 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66410-24:
(7*6)+(6*6)+(5*4)+(4*1)+(3*0)+(2*2)+(1*4)=110
110 % 10 = 0
So 66410-24-0 is a valid CAS Registry Number.
66410-24-0Relevant articles and documents
Method for preparation of Octadecadienyl acetate as major sex pheromone of cherry tree borer, Synanthedon bicingulate
-
, (2018/06/26)
The present invention relates to a method for producing a sex pheromone of cherry tree borer (Synanthedon bicingulata) in an attempt to control the same. More specifically, provided is a method for stereoselectively producing high purity (3E,13Z)- octadecadienyl acetate and (3Z,13Z)-octadecadienyl acetate respectively which are major sex pheromones of cherry tree borer from a cheap starting material in an efficient, simple, and economically feasible way.COPYRIGHT KIPO 2018
Synthesis of (3Z,13Z)-3,13-octadecadienyl acetate - Sex pheromone of Synanthedon tenuis-using readily available C11-synthon
Narasimhan,Ganeshwar Prasad,Madhavan
, p. 99 - 101 (2007/10/03)
Synthesis of (3Z,13Z)-3,13-octadecadienyl acetate has been achieved from the readily available 10-undecen-1-ol using cheaper reagents and less number of steps. In the key step alkylation of an alkyne is performed with solid sodamide giving the product in 50% yield. The method can be easily scaled-up.
1,(ω-1)-Dienes: solvent controlled unilateral or bilateral metallation
Moret, Etienne,Desponds, Olivier,Schlosser, Manfred
, p. 83 - 91 (2007/10/02)
In hexane, i.e. under heterogeneous conditions, 1,(ω-1)-dienes readily undergo double deprotonation to give bis(allylmetal) intermediates.In tetrahydrofuran at -75 or -50 deg C, however, only monometallation occurs with dienes having chains of up to 12 carbon atoms.The practical potential of such selective monosubstitution reactions is demonstrated by two novel pheromone syntheses.
