37011-95-3 Usage
Description
(E)-7-Tetradecen-1-ol, also known as Z-7-tetradecen-1-ol, is a primary alcohol with a double bond in the (E)-configuration at the 7th carbon position. It is a naturally occurring organic compound that can be found in various plant species and is known for its distinct chemical properties and potential applications.
Uses
Used in Analytical Chemistry:
(E)-7-Tetradecen-1-ol is used as a reference compound for determining Kovats indexes, which are essential for providing an unambiguous identification of volatile organic compounds in gas chromatography. (E)-7-Tetradecen-1-ol's unique chemical structure and properties make it a valuable tool in the field of analytical chemistry for characterizing and identifying various substances.
Used in Flavor and Fragrance Industry:
(E)-7-Tetradecen-1-ol is used as a key component in the synthesis of various fragrances and flavors. Its unique olfactory properties contribute to the development of new and innovative scents for the perfumery and flavor industries, enhancing the sensory experience of consumers.
Used in Pheromone Research:
(E)-7-Tetradecen-1-ol has been identified as a component in the pheromone blends of certain insects, making it an important compound in the study of chemical communication and mating behavior in the animal kingdom. Researchers use this compound to better understand the role of pheromones in attracting mates and the underlying mechanisms of these biological processes.
Used in Biotechnology:
The unique chemical properties of (E)-7-Tetradecen-1-ol also make it a potential candidate for use in biotechnological applications, such as the development of novel bioactive compounds or the enhancement of existing ones. Its ability to interact with other molecules and its potential for modification make it a promising starting point for the creation of new bioproducts.
Check Digit Verification of cas no
The CAS Registry Mumber 37011-95-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,1 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37011-95:
(7*3)+(6*7)+(5*0)+(4*1)+(3*1)+(2*9)+(1*5)=93
93 % 10 = 3
So 37011-95-3 is a valid CAS Registry Number.
37011-95-3Relevant articles and documents
Iron thiolate complexes: Efficient catalysts for coupling alkenyl halides with alkyl grignard reagents
Cahiez, Gerard,Gager, Olivier,Buendia, Julien,Patinote, Cindy
supporting information; experimental part, p. 5860 - 5863 (2012/07/01)
Ironing out the kinks: Efficient new catalytic systems based on iron thiolates are described for the iron-catalyzed cross-coupling of alkyl Grignard reagents with alkenyl halides (see scheme). The reaction is highly chemo- and stereoselective. With this new procedure, the use of N-methylpyrrolidone as a co-solvent is no longer required. Copyright
Sex pheromone of female vine bud moth, Theresimima ampellophaga comprises (2s)-butyl (7z)-tetradecenoate
Subchev,Harizanov,Francke,Franke,Plass,Reckziegel,Schroeder,Pickett,Wadhams,Woodcock
, p. 1141 - 1151 (2007/10/03)
The sex pheromone of the vine bud moth, Theresimima ampellophaga, released at the 3rd-5th abdominal tergites, was identified by coupled GC-EAG, GC-MS, and synthesis as (2S)-butyl (7Z)-tetradecenoate. For the first time, full stereochemistry is unambiguously defined for the sex pheromone of a member of the Zygaenidae. The synthetic compound caught significant numbers of males in field-trapping experiments.
STEREOSPECIFIC SYNTHESIS OF PHEROMONES OF THE E-ALKENE SERIES FROM THE TELOMER OF BUTADIENE WITH PHENOL
Zakharkin, L. I.,Petrushkina, E. A.
, p. 1419 - 1422 (2007/10/02)
The stereospecific synthesis of 7E- and 9E-dodecenyl acetates, 7E- and 11E-tetradecenyl acetates, 11E-tetradecen-1-ol, and 11E-hexadecenyl acetate, i.e., E-olefinic sex pheromones, was realized from 1-phenoxy-2E,7-octadiene (the telomer of butadiene with phenol).
