929-55-5 Usage
Description
(1E)-octanal oxime, with the molecular formula C8H17NO, is an oxime derivative of octanal. It is a chemical compound that can be found in many essential oils and is known for its use as a flavoring agent and fragrance. (1E)-octanal oxime has garnered interest due to its potential applications in various fields, including pharmaceuticals, organic synthesis, and as a chelating agent in coordination chemistry.
Uses
Used in Pharmaceutical Industry:
(1E)-octanal oxime is used as a pharmaceutical agent for its anti-inflammatory properties. It has been investigated for its potential to treat various medical conditions, making it a valuable compound in the development of new medications.
Used in Flavor and Fragrance Industry:
As a derivative of octanal, (1E)-octanal oxime is used as a flavoring agent and fragrance. Its presence in essential oils contributes to the unique scents and tastes in a variety of products, from food to cosmetics.
Used in Organic Synthesis:
(1E)-octanal oxime serves as a building block for the synthesis of other organic compounds. Its versatility in chemical reactions makes it a useful component in creating new and complex molecules for various applications.
Used in Coordination Chemistry:
(1E)-octanal oxime is utilized as a chelating agent in coordination chemistry. This role allows it to form stable complexes with metal ions, which can be important in various chemical and material science applications.
Used in Heterocyclic Compound Synthesis:
(1E)-octanal oxime has been employed in the synthesis of heterocyclic compounds, which are an important class of organic compounds with diverse applications in pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 929-55-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 929-55:
(5*9)+(4*2)+(3*9)+(2*5)+(1*5)=95
95 % 10 = 5
So 929-55-5 is a valid CAS Registry Number.
929-55-5Relevant articles and documents
Hydroxylamine Reactions with Peroxide Products of Alkenes Ozonolysis
Legostaeva, Yu. V.,Garifullina,Nazarov,Ishmuratova,Ishmuratov, G. Yu.
, p. 1122 - 1126 (2018/10/24)
Reactions were studied of peroxide ozonolysis products obtained from linear and cyclic alkenes with hydroxylamine prepared in situ from NH2OH·HCl by hydrogen chloride neutralization with sodium acetate. A one-pot reactions sequence was performed: alkene oxidation with ozone → reduction to a carbonyl compound with hydroxylamine → condensation of the carbonyl compound with hydroxylamine providing a possibility of direct transformation of alkenes in keto- and aldoximes excluding the stage of preparation and isolation of the carbonyl compound.
Intermolecular cope-type hydroamination of alkenes and alkynes
Beauchemin, Andre M.,Moran, Joseph,Lebrun, Marie-Eve,Seguin, Catherine,Dimitrijevic, Elena,Zhang, Lili,Gorelsky, Serge I.
, p. 1410 - 1413 (2008/12/23)
(Chemical Equation Presented) Keep it simple! Intermolecular hydroamination can be achieved simply upon heating alkynes and alkenes with aqueous hydroxylamine. Alkynes react to afford oximes in good to excellent yields, and the formation of Markovnikov products is favored. A mechanism involving Cope-type hydroamination followed by bimolecular proton transfer is suggested and supported by DFT studies.
Facile conversion of acetals to nitriles
Yamauchi
, p. 2042 - 2043 (2007/10/02)
Aliphatic and aromatic acetals are easily and efficiently converted to the corresponding nitriles by reaction with hydroxylamine hydrochloride in refluxing absolute ethanol.
