57322-44-8 Usage
Uses
Used in Pharmaceutical Industry:
(1-METHYLNAPHTHALEN-4-YL)METHANOL is used as an intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, (1-METHYLNAPHTHALEN-4-YL)METHANOL serves as an intermediate for the synthesis of agrochemicals, contributing to the development of products that enhance crop protection and yield.
Used in Specialty Chemicals Industry:
(1-METHYLNAPHTHALEN-4-YL)METHANOL is utilized as a building block in the synthesis of specialty chemicals, which are tailored for specific applications in various industries, such as coatings, adhesives, and plastics.
Used in Fragrance and Flavor Industry:
Due to its aromatic properties, (1-METHYLNAPHTHALEN-4-YL)METHANOL may have potential uses in the manufacturing of fragrances and flavors, adding unique scents and tastes to various consumer products.
Safety Note:
It is important to handle (1-METHYLNAPHTHALEN-4-YL)METHANOL with caution, as it may pose health and environmental hazards. Proper safety measures should be taken during its production, use, and disposal to minimize any potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 57322-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,2 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57322-44:
(7*5)+(6*7)+(5*3)+(4*2)+(3*2)+(2*4)+(1*4)=118
118 % 10 = 8
So 57322-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O/c1-9-6-7-10(8-13)12-5-3-2-4-11(9)12/h2-7,13H,8H2,1H3
57322-44-8Relevant 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
187. Acid-Catalyzed Cleavage of 1,4-Dimethyl-1,4-dihydronaphthalene 1,4-Endoperoxide. Reactivity of the Resulting Hydroxyperoxy Carbocation with Nucleophiles
Jefford, Charles W.,Rossier, Jean-Claud,Kohmoto, Shigeo,Boukouvalas, John
, p. 1804 - 1814 (2007/10/02)
In the presence of acids, 1,4-dimethyl-1,4-dihydronaphthalene 1,4-endoperoxie readily reacts with nucleophiles to produce methyl- and ring-substituted naphthalenes in high yields.The regioselectivity observed depends on the nucleophile.The key intermediate is shown to be the corresponding hydroperoxy carbocation which could be intercepted in certain cases prior to aromatization.The hydroperoxide also undergoes Hock-type cleavage and dimerization giving 2,3-dihydro-1-benzoxepins, 4-methyl-1-naphthol, and 1,2,5,6-tetraoxocane as by-products.
