33738-48-6 Usage
Description
4-METHYL-1-NAPHTHALDEHYDE, also known as a monoaldehyde, is an organic compound derived from 1-methylnaphthalene through a formylation process. It is characterized by its distinct chemical structure and properties, making it a versatile compound for various applications.
Uses
Used in Chemical Synthesis:
4-METHYL-1-NAPHTHALDEHYDE is used as a key intermediate in the synthesis of various organic compounds for different applications. It serves as a building block for creating complex molecules with specific properties and functions.
Used in Pharmaceutical Industry:
4-METHYL-1-NAPHTHALDEHYDE is used as a starting material for the synthesis of methyl 2-phenyl-3-(4-methyl-1-naphthyl)propenoate, which may have potential applications in the development of pharmaceutical compounds.
Used in Chemical Research:
4-METHYL-1-NAPHTHALDEHYDE is used as a research compound in the development of new chemical reactions and methodologies. Its unique structure allows chemists to explore novel synthetic pathways and improve existing ones.
Used in Material Science:
4-METHYL-1-NAPHTHALDEHYDE is used in the synthesis of (Z/E)-2-amino-4,6-dimethyl-5-[(4-methyl-1-naphthyl)methylene]-5H-cyclopenta[b]pyridine-3,7-dicarbonitrile, which may have potential applications in the development of new materials with specific properties, such as optoelectronic devices or advanced polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 33738-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,3 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33738-48:
(7*3)+(6*3)+(5*7)+(4*3)+(3*8)+(2*4)+(1*8)=126
126 % 10 = 6
So 33738-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O/c1-9-6-7-10(8-13)12-5-3-2-4-11(9)12/h2-8H,1H3
33738-48-6Relevant articles and documents
Controlled photochemical release of nitric oxide from O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates
Bushan, K. Mani,Xu, Hua,Ruane, Patrick H.,D'Sa, Raechelle A.,Pavlos, Christopher M.,Smith, Joseph A.,Celius, Tevye C.,Toscano, John P.
, p. 12640 - 12641 (2007/10/03)
The photochemistry of O2-naphthylmethyl- and O2-naphthylallyl-substituted diazeniumdiolates has been investigated. Electron-donating methoxy group substitution is shown to have a significant effect on the observed photochemistry, with the appropriate substitution pattern resulting in efficient diazeniumdiolate photorelease. Observed nitric oxide release rates from these photoprecursors are consistent with those expected for normal thermal dissociation of the diazeniumdiolate in aqueous solutions and show the same pH dependence. Copyright
The influence of aromatic compound protonation on the regioselectivity of Gattermann-Koch formylation
Tanaka, Mutsuo,Fujiwara, Masahiro,Ando, Hisanori,Souma, Yoshie
, p. 159 - 160 (2007/10/03)
The regioselectivity of the Gattermann-Koch formylation is influenced by the protonation of aromatic compounds under a solvent-cage-like atmosphere.
ELECTRON TRANSFER ACTIVATION. HYDROPEROXIDE INTERMEDIATES IN A NOVEL AND SELECTIVE PROCEDURE FOR BENZYLIC OXIDATIONS.
Santamaria, J.,Jroundi, R.,Rigaudy, J.
, p. 4677 - 4680 (2007/10/02)
A selective and mild photochemical procedure for benzylic oxidations with 9,10-dicyanoanthracene (DCA) an usual electron acceptor, in the presence of methyl viologen (MV2+), an electron relay, has been developed.Methyl and methylene groups are oxidized in good to excellent yields to the corresponding hydroperoxides.
