81259-54-3 Usage
General Description
4-(Benzyloxy)-3-methoxybenzaldehyde oxime is a chemical compound with the molecular formula C15H15NO3. It is an oxime derivative of benzaldehyde and contains a benzyl ether group and a methoxy group. Benzaldehyde oximes are known for their potential use in the synthesis of various pharmaceuticals and other organic compounds. Oximes are often used in organic chemistry as intermediates in the synthesis of complex molecules and as reagents in various reactions. 4-(BENZYLOXY)-3-METHOXYBENZALDEHYDE OXIME may have potential applications in the pharmaceutical and chemical industries due to its reactivity and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 81259-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81259-54:
(7*8)+(6*1)+(5*2)+(4*5)+(3*9)+(2*5)+(1*4)=133
133 % 10 = 3
So 81259-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H15NO3/c1-18-15-9-13(10-16-17)7-8-14(15)19-11-12-5-3-2-4-6-12/h2-10,17H,11H2,1H3/b16-10-
81259-54-3Relevant articles and documents
Solvent free, microwave assisted conversion of aldehydes into nitriles and oximes in the presence of NH2OH · HCl and TiO2
Hoelz, Lucas Villas-Boas,Goncalves, Biank Tomaz,Barros, Jose Celestino,Silva, Joaquim Fernando Mendes Da
experimental part, p. 94 - 99 (2010/05/18)
Aromatic aldehydes bearing electron-donating groups are easily converted into their respective nitriles using NH2OH · HCl and TiO 2 under microwave irradiation, while those bearing an electron-withdrawing group give the corresponding oximes.
Synthesis of new 4,5-dihydroisoxazoles with potential anti-inflammatory activity
Molina, Cleia Tomaz,De Aguiar, Alcino Palermo
, p. 535 - 538 (2007/10/03)
This paper reports the synthesis of different 4,5-dihydroisoxazoles which may present anti-inflammatory activity. The methodology employed was based on the 1,3-dipolar cycloaddition of nitrile oxide derived from vanillin to unsaturated compounds. It was u
