71084-08-7 Usage
Uses
Used in Chemical Synthesis:
9-Dodecyn-1-ol is used as a precursor in the synthesis of pharmaceuticals, fragrances, and flavoring agents due to its versatile chemical properties.
Used in Nanotechnology:
9-Dodecyn-1-ol is used in the field of nanotechnology for the fabrication of nanostructured materials and as a stabilizing agent for metal nanoparticles, taking advantage of its unique molecular structure.
Used in Personal Care and Cosmetic Products:
9-Dodecyn-1-ol is used as an ingredient in personal care and cosmetic products due to its antimicrobial and antibacterial properties, which contribute to the formulation's effectiveness and safety.
Used in Surfactant Production:
9-Dodecyn-1-ol is used as a component in the production of surfactants, which are essential in various industries for their ability to reduce surface tension and create stable emulsions.
Used in Lubricant Formulation:
9-Dodecyn-1-ol is used in the formulation of lubricants, where its properties can enhance the performance and longevity of the lubricating products.
Used in Pharmaceutical Industry:
9-Dodecyn-1-ol is used as a precursor in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Overall, 9-Dodecyn-1-ol is a versatile chemical compound with various industrial and scientific applications, including chemical synthesis, nanotechnology, personal care, surfactant production, lubricant formulation, and pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 71084-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,8 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71084-08:
(7*7)+(6*1)+(5*0)+(4*8)+(3*4)+(2*0)+(1*8)=107
107 % 10 = 7
So 71084-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h13H,2,5-12H2,1H3
71084-08-7Relevant academic research and scientific papers
Pheromones of insects and their analogs. LII. Sythesis of dodec-9-en-1-yl and tetradec-11-en-1-yl acetates from the products of the partial ozonolysis of cycloocta-1z,5z-diene and cyclodeca-1e,5z-diene
Odinokov,Botsman,Gladysheva
, p. 381 - 383 (2007/10/03)
A new approach to the synthesis of octane-1,8-and decane-1,10-diols based on the partial ozonolysis of cyclic oligomers has been developed.
Synthesis of (S,E)-1-Methyl-9-dodecenyl Acetate, the Sex Pheromone of the Hessian Fly, Mayetiola destructor, by Lipase-catalyzed Enantioselective Hydrolysis
Kamezawa, Makoto,Tachibana, Hojun,Ohtani, Takehiko,Naoshima, Yoshinobu
, p. 1962 - 1963 (2007/10/02)
(S,E)-1-Methyl-9-dodecenyl acetate , the sex pheromone of the hessian fly, Mayetiola destructor, was synthesized in a highly enantiomerically pure form by Pseudomonas cepacia lipase-catalyzed hydrolysis.
