821-97-6 Usage
Description
(Z)-3-Undecene, a colorless liquid hydrocarbon with the molecular formula C11H22, is an unsaturated alkene compound featuring a double bond in the cis configuration. It is recognized for its distinctive odor and serves as a crucial chemical intermediate in the synthesis of a wide array of products, including fragrances, flavors, and polymers.
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 articles and documents
The catalytic Shapiro reaction
Maruoka, Keiji,Oishi, Masataka,Yamamoto, Hisashi
, p. 2289 - 2290 (2007/10/03)
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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.
DECARBOXYLATION OF ALIPHATIC α,β-UNSATURATED ALDEHYDES USING THE WILKINSON COMPLEX
Grigor'eva, N. Ya.,Pinsker, O. A.,Semenovskii, A. V.
, p. 593 - 594 (2007/10/02)
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