39110-92-4 Usage
Uses
Used in Pharmaceutical Industry:
3-METHOXY-2-NAPHTHALENEMETHANOL 97 is used as an intermediate compound for the synthesis of various pharmaceuticals and drug candidates. Its unique chemical structure allows it to be a key component in the development of new medications with potential therapeutic benefits.
Used in Chemical Synthesis:
In the field of organic chemistry, 3-METHOXY-2-NAPHTHALENEMETHANOL 97 is used as a starting material or intermediate for the synthesis of a wide range of chemical compounds. Its reactivity and functional groups make it a versatile building block for creating complex molecules with specific properties and applications.
Used in Research and Development:
3-METHOXY-2-NAPHTHALENEMETHANOL 97 is also utilized in research and development laboratories for studying its chemical properties, reactivity, and potential applications in various fields. Scientists and researchers use 3-METHOXY-2-NAPHTHALENEMETHANOL 97 to explore new reaction pathways, develop novel synthetic methods, and investigate its potential as a precursor for other valuable chemicals.
Specific Application:
3-METHOXY-2-NAPHTHALENEMETHANOL 97 is used as a synthetic intermediate for the production of 2-carbomethoxy-4-methoxy-6,7-benzoindole, a compound with potential applications in various industries, including pharmaceuticals and materials science. The synthesis of 3-METHOXY-2-NAPHTHALENEMETHANOL 97 demonstrates the versatility and utility of 3-METHOXY-2-NAPHTHALENEMETHANOL 97 in creating complex and valuable molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 39110-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39110-92:
(7*3)+(6*9)+(5*1)+(4*1)+(3*0)+(2*9)+(1*2)=104
104 % 10 = 4
So 39110-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O2/c1-14-12-7-10-5-3-2-4-9(10)6-11(12)8-13/h2-7,13H,8H2,1H3
39110-92-4Relevant academic research and scientific papers
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
