821-97-6 Usage
Uses
Used in the Fragrance Industry:
(Z)-3-Undecene is used as a chemical intermediate for creating various fragrances, capitalizing on its characteristic odor to enhance the scent profiles of different products.
Used in the Flavor Industry:
It is also utilized as a building block in the flavor industry, where its unique properties contribute to the development of novel and complex taste sensations.
Used in the Polymer Industry:
(Z)-3-Undecene is used as a chemical intermediate in the production of polymers, which are essential materials in a multitude of applications, from plastics to coatings.
Used in the Specialty Chemicals Industry:
(Z)-3-Undecene is employed as a chemical building block in the production of specialty chemicals, where its versatile nature allows for the creation of a broad spectrum of high-value products.
Used in the Insect Pheromone Industry:
(Z)-3-Undecene is used as a component in the synthesis of insect pheromones, which are crucial for various applications such as pest control and ecological research.
Used in the Lubricant and Fuel Additives Industry:
It is also utilized as a component in lubricant and fuel additives, where its properties can improve the performance and efficiency of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 821-97-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 821-97:
(5*8)+(4*2)+(3*1)+(2*9)+(1*7)=76
76 % 10 = 6
So 821-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H22/c1-3-5-7-9-11-10-8-6-4-2/h5,7H,3-4,6,8-11H2,1-2H3/b7-5-
821-97-6Relevant academic research and scientific papers
Hindered organoboron groups in organic chemistry. 25. The condensation of aliphatic aldehydes with dimesitylboryl stabilised carbanions to give alkenes
Pelter,Smith,Elgendy
, p. 7119 - 7132 (2007/10/02)
In the presence of protic acids the condensation of aliphatic aldehydes with dimesitylboryl stabilised carbanions results in alkenes. In the presence of strong acids such as HCl or CF3SO3H, the products contain > 90% of E-alkenes in all cases tried. When acetic acid is used, the Z-alkenes may result predominantly, particularly in the cases of R(S)CHO and R(t)CHO.
HINDERED ORGANOBORON GROUPS IN ORGANIC SYNTHESIS. 14. STEREOSELECTIVE SYNTHESIS OF ALKENES BY THE BORON-WITTIG REACTION USING ALIPHATIC ALDEHYDES
Pelter, Andrew,Smith, Keith,Elgendy, Said,Rowlands, Martin
, p. 5647 - 5650 (2007/10/02)
In the presence of HX, carbanions Mes2BCHLiR1 react with aliphatic aldehydes to give alkenes.The stereochemistry of product alkene depends upon the nature of HX.
HINDERED ORGANOBORON GROUPS IN ORGANIC SYNTHESIS. 13. THE DIRECT PRODUCTION OF KETONES FROM ALIPHATIC ALDEHYDES BY A UNIQUE VARIANT OF THE BORON-WITTIG REACTION
Pelter, Andrew,Smith, Keith,Elgendy, Said,Rowlands, Martin
, p. 5643 - 5646 (2007/10/02)
In the presence of trifluoroacetic anhydride or N-chlorosuccinimide, aliphatic aldehydes react with dimesitylboron stabilised carbanions to give after work up, the corresponding ketones, a process wich is unique among Wittig type reactions.Yields of ketones are satisfactory in all cases except those involving the anion derived from the parent compound dimesitylmethylborane, wich give the corresponding alkenes.
