35329-50-1 Usage
Description
(E)-4-Nonenoic acid, also known as non-4-enoic acid, is a chemical compound with the molecular formula C9H16O2. It is a carboxylic acid that exists as a colorless to pale yellow liquid with a fruity, waxy odor. (E)-4-Nonenoic acid is insoluble in water but soluble in organic solvents, making it versatile for various applications.
Uses
Used in Flavor and Fragrance Industry:
(E)-4-Nonenoic acid is used as a flavoring agent in the food and beverage industry, adding unique fruity and waxy notes to enhance the overall taste and aroma of products. Its ability to dissolve in organic solvents makes it an ideal candidate for these applications.
Used in Chemical Synthesis:
(E)-4-Nonenoic acid serves as a chemical intermediate in the synthesis of other organic compounds. Its carboxylic acid structure allows for further reactions and modifications, contributing to the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
(E)-4-Nonenoic acid has potential applications in the pharmaceutical industry, particularly in the development of drugs and medicines. Its chemical properties and solubility in organic solvents make it a promising candidate for research and development in medicinal chemistry.
Used in Perfumery:
(E)-4-Nonenoic acid is also a component in the production of fragrances and perfumes, where its fruity and waxy odor adds depth and complexity to the final scent. Its solubility in organic solvents facilitates its incorporation into various perfume formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 35329-50-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,2 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35329-50:
(7*3)+(6*5)+(5*3)+(4*2)+(3*9)+(2*5)+(1*0)=111
111 % 10 = 1
So 35329-50-1 is a valid CAS Registry Number.
35329-50-1Relevant articles and documents
An Efficient Route for γ-Alkyl-γ-butyrolactones
Gurjar, M. K.,Purandare, A. V.
, p. 554 - 555 (2007/10/02)
An efficient route for γ-alkyl-γ-butyrolactones (1) involving iodolactonisation is described.
New Synthetic Methods, 12. - The Stereoselectivity of the Ramberg-Baecklund Rearrangement
Scholz, Dieter,Burtscher, Peter
, p. 517 - 521 (2007/10/02)
The influence of strong and weak bases in different solvents on the (E)/(Z) ratio of the Ramberg-Baecklund olefin synthesis of α-halosulfoncarboxylic acids in studied.With potassium tert-butoxide in dry dimethyl sulfoxide (E) ratios of more than 97 percent are achieved.With weak bases, such as 0.25 N sodium hydroxide, we found only equal amounts of (E) and (Z) olefins, apart from a few exceptions.
Neue Synthesemethoden, 3. Tetrahydrothiopyran-3-on-1,1-dioxid, ein nuetzlicher 4-C-Baustein zur stereoselektiven Synthese von (Z)- oder (E)-γ,δ-ungesaettigten Carbonsaeuren
Scholz, Dieter
, p. 909 - 915 (2007/10/02)
By alkylation and ring opening together with bromination, tetrahydrothiopyran-3-one 1,1-dioxide (2) is converted into α-halosulfone intermediates, which can be transformed stereoselectively by Ramberg-Backlund rearrangement to (Z)- or (E)-γ,δ-unsaturated
