78910-33-5 Usage
Description
2,4-Decadienoic acid pyrrolidide is a chemical compound characterized by its light orange to brown color and low melting solid properties. It is derived from the 2,4-decadienoic acid and has a pyrrolidide functional group attached to it, which contributes to its unique chemical and physical characteristics.
Uses
Used in Pest Control Industry:
2,4-Decadienoic acid pyrrolidide is used as a biopesticide for controlling plant pests. Its chemical properties allow it to effectively target and manage various pests that can damage crops and reduce agricultural productivity. 2,4-Decadienoic acid pyrrolidide's low melting point enables it to be easily formulated and applied to plants, providing a practical and efficient solution for pest management.
Used in Chemical Synthesis:
In the chemical industry, 2,4-Decadienoic acid pyrrolidide can be utilized as an intermediate in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable building block for creating a wide range of products, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Flavor and Fragrance Industry:
Due to its distinct chemical properties, 2,4-Decadienoic acid pyrrolidide can also be employed in the flavor and fragrance industry. It can be used as a key ingredient in the development of new and innovative scents, as well as in the enhancement of existing fragrances. Its unique chemical structure contributes to the creation of complex and nuanced aromas that can be used in various applications, such as perfumes, cosmetics, and household products.
Used in Material Science:
The low melting point and unique chemical properties of 2,4-Decadienoic acid pyrrolidide make it a potential candidate for use in the development of new materials with specific properties. It can be incorporated into polymers, coatings, and other materials to enhance their performance characteristics, such as improved thermal stability, enhanced mechanical properties, or increased resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 78910-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78910-33:
(7*7)+(6*8)+(5*9)+(4*1)+(3*0)+(2*3)+(1*3)=155
155 % 10 = 5
So 78910-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H23NO/c1-2-3-4-5-6-7-8-11-14(16)15-12-9-10-13-15/h6-8,11H,2-5,9-10,12-13H2,1H3/b7-6+,11-8+
78910-33-5Relevant articles and documents
Iron-Catalyzed Synthesis of Sarmentine
Ignatishina, M. G.,Shakhmaev, R. N.,Zorin, V. V.
, p. 1002 - 1005 (2021/07/22)
Abstract: Stereoselective synthesis of sarmentine has been achieved via iron-catalyzed cross-coupling of pentylmagnesium bromide with ethyl (2E,4E)-5-chloropenta-2,4-dienoate obtained by one-pot oxidation–olefination of readily available (2E)-3-chloroprop
Stereoselective synthesis of sarmentine
Shakhmaev,Ishbaeva,Sunagatullina,Zorin
experimental part, p. 1915 - 1917 (2012/01/07)
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Stereoselective synthesis of naturally occurring unsaturated amide alkaloids by a modified Ramberg-Baecklund reaction
Li, Yang,Zhang, Yu,Huang, Zhi,Cao, Xiaoping,Gao, Kun
, p. 622 - 630 (2007/10/03)
A convenient and rapid approach for the synthesis of naturally occurring unsaturated amide alkaloids 1a-1n by the recently developed one-flask Ramberg-Baecklund reaction is described. The starting material was alcohol 3, which was transformed into thiolacetate 4 using the Mitsunobu reaction. In situ cleavage of acetyl moiety of 4, followed by alkylation of the resulting thiol with appropriate chloroacetamide 5, provided the sulfide 6. Oxidation of sulfide 6 gave the corresponding sulfone 2. Treatment of the sulfone 2 with the dibromodifluoromethane in the presence of alumina-supported potassium hydroxide in dichloromethane solution afforded unsaturated amide alkaloids 1a-1n. To the best of our knowledge, the synthesis of 1e and 1i was reported for the first time.
