21944-83-2 Usage
Description
3,6-nonadienal,(Z,Z)-3,6-nonadienal, also known as cis,cis-3,6-Nonadienal, is a volatile compound found in cucumber. It is derived from the biosynthesis of linolenic and linoleic acids, which are essential fatty acids. 3,6-nonadienal,(Z,Z)-3,6-nonadienal has a unique chemical structure and properties that make it a valuable subject for research and potential applications.
Uses
Used in Agricultural Research:
3,6-nonadienal,(Z,Z)-3,6-nonadienal is used as a research compound for investigating biosynthesis pathways in cucumber. Its presence in cucumber suggests that it plays a role in the plant's metabolic processes, and studying its synthesis can provide insights into the plant's growth and development.
Used in Flavor and Fragrance Industry:
3,6-nonadienal,(Z,Z)-3,6-nonadienal is used as a flavoring agent and fragrance ingredient due to its distinct aroma and taste. Its volatile nature allows it to impart a unique scent and flavor to various products, making it a valuable component in the creation of perfumes, cosmetics, and food products.
Used in Analytical Chemistry:
3,6-nonadienal,(Z,Z)-3,6-nonadienal can be used as an analytical standard in chemical analysis. Its unique chemical properties make it a useful reference compound for the development and calibration of analytical methods, such as gas chromatography and mass spectrometry, which are used to identify and quantify volatile compounds in various samples.
Check Digit Verification of cas no
The CAS Registry Mumber 21944-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21944-83:
(7*2)+(6*1)+(5*9)+(4*4)+(3*4)+(2*8)+(1*3)=112
112 % 10 = 2
So 21944-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O/c1-2-3-4-5-6-7-8-9-10/h3-4,6-7,9H,2,5,8H2,1H3/b4-3-,7-6-
21944-83-2Relevant articles and documents
Easy access to aroma active unsaturated γ-lactones by addition of modified titanium homoenolate to aldehydes
Frerot, Eric,Bagnoud, Alain
experimental part, p. 4057 - 4061 (2011/10/31)
The homo-Reformatsky reaction, in which a metal homoenolate of an ester is added to an aldehyde, was adapted to produce γ-lactones from unsaturated, enolizable aldehydes. By use of titanium homoenolate, 11 different γ-lactones were synthesized in one step with moderate to good yields from readily available aldehydes. In particular, this procedure allowed the rapid preparation of a series of C12 unsaturated γ-lactones differing in the position and configuration of the double bond. These reference compounds will be used to identify previously unknown lactones in butter oil. The chromatographic, spectral, and sensory descriptions of the synthesized lactones are provided.
