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(E)-5-Nonenal, also known as trans-5-nonenal, is an organic compound with the chemical formula C9H16O. It is a positional isomer of nonanal, an aldehyde with a nine-carbon chain. This colorless liquid has a strong, pungent odor and is commonly found in various natural sources, such as fruits, vegetables, and human sweat. (E)-5-Nonenal is an important contributor to the odor of aged and rancid foods, as well as the characteristic smell of human skin. It is also used as a fragrance ingredient in the perfume industry and as a flavoring agent in food products. Due to its reactive nature, (E)-5-Nonenal can undergo various chemical reactions, such as oxidation and reduction, making it a versatile compound in organic chemistry.

2277-18-1

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2277-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2277-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2277-18:
(6*2)+(5*2)+(4*7)+(3*7)+(2*1)+(1*8)=81
81 % 10 = 1
So 2277-18-1 is a valid CAS Registry Number.

2277-18-1Relevant academic research and scientific papers

Treasures from the Free Radical Renaissance Period - Miscellaneous hexenyl radical kinetic data

Beckwith, Athelstan L. J.,Schiesser, Carl H.

experimental part, p. 1736 - 1743 (2011/05/03)

Rate constant data and Arrhenius parameters have been determined for a series of substituted hexenyl radicals of differing electronic and steric demand. Electron-withdrawing groups (CF3, CO2Et) directly attached to the radical centre slighly accelerate 5-exo ring-closure (k cis + ktrans ~ 2.1 × 105 s -1 at 25°) relative to donating groups (OMe; 1.6 × 10 5 s-1 at 25°). Sterically demanding groups (tert-Bu), as expected, slow the cyclization process (1 × 105 s -1). These observations are consistent with subtle changes in activation energy for 5-exo ring-closure. Interestingly, the nature of the solvent would appear to have a significant influence on this chemistry with the cis/trans stereoselectivity sometimes improved as the solvent polarity is increased. Except for the system containing the CF3 (electron-withdrawing) group which displays an increase in the cyclization/capture rate constant (kc/kH), a general decrease in the kc/kH ratio as solvent polarity is increased is noted; these changes have been speculated to arise mainly from changes in kH in the various solvents employed.

PROCESS FOR THE DIRECT CONVERSION OF LACTONES INTO UNSATURATED KETONES OR ALDEHYDES

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Page 10, (2008/06/13)

The present invention refers to a process for the preparation of unsaturated ketones or aldehydes by pyrolysis of a lactone, in the presence of a reducing agent such as molecular hydrogen or a carboxylic acid, and in the presence of a catalyst, optionally

Synergistic sex pheromone components of white-spotted tussock moth, Orgyia thyellina

Gries, Gerhard,Clearwater, John,Gries, Regine,Khaskin, Grigori,King, Skip,Schaefer, Paul

, p. 1091 - 1104 (2007/10/03)

In 1996, the exotic white-spotted tussock moth (WSTM), Orgyia thyellina (Lepidoptera: Lymantriidae), was discovered in Auckland, New Zealand. Because establishment of WSTM would threaten New Zealand's orchard industry and international trade, eradication of WSTM with microbial insecticide was initiated. To monitor and complement eradication of WSTM by capture of male moths in pheromone-baited traps, pheromone components of female WSTM needed to be identified. Coupled gas chromatographic-electroantennographic detection analysis of pheromone gland extract revealed several compounds that elicited responses from male moth antennae. Mass spectra of the two most EAD-active compounds suggested, and comparative GC-MS of authentic standards confirmed, that they were (Z)-6-heneicosen-11-one (Z6-11-one) and (Z)-6-heneicosen-9- one, the latter termed here 'thyellinone.' In field experiments in Japan, Z6- 11-one plus thyellinone at a 100:5 ratio attracted WSTM males, whereas either ketone alone failed to attract a single male moth. Addition of further candidate pheromone components did not enhance attractiveness of the binary blend. Through the 1997-1998 summer, 45,000 commercial trap lures baited with 2000 μg of Z6-11-one and 100 μg of thyellinone were deployed in Auckland towards eradication of the residual WSTM population.

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