17579-79-2 Usage
Description
6-METHYL-2-NAPHTHOL, also known as 6-Methylnaphthalen-2-ol, is an organic compound with the molecular formula C11H10O. It is a white crystalline solid that is soluble in organic solvents and has a distinct chemical structure featuring a naphthalene ring with a methyl group at the 6th position and a hydroxyl group at the 2nd position.
Uses
Used in Pharmaceutical Industry:
6-METHYL-2-NAPHTHOL is used as a reactant for the preparation of dioncoquinone derivatives, which possess anti-tumoral activities. These derivatives have the potential to be developed into pharmaceutical compounds for the treatment of various types of cancer.
Used in Chemical Synthesis:
6-METHYL-2-NAPHTHOL can also be utilized as a building block or intermediate in the synthesis of various organic compounds, including dyes, pigments, and other specialty chemicals. Its unique chemical structure allows for further functionalization and modification to create a wide range of products with different applications.
Purification Methods
Crystallise the naphthol from EtOH or ligroin. Sublime it in vacuo.[Beilstein 6 II 618, 6 III 3028.]
Check Digit Verification of cas no
The CAS Registry Mumber 17579-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17579-79:
(7*1)+(6*7)+(5*5)+(4*7)+(3*9)+(2*7)+(1*9)=152
152 % 10 = 2
So 17579-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O/c1-8-2-3-10-7-11(12)5-4-9(10)6-8/h2-7,12H,1H3
17579-79-2Relevant articles and documents
Shreve,Lloyd
, p. 811 (1950)
SMALL MOLECULE INHIBITORS OF A PROTEIN COMPLEX
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Paragraph 00165, (2020/12/29)
Compositions and methods for treating thrombosis, inflammation, and atherosclerosis by administration of a compound that binds to KRIT1 to inhibit binding with HEG1.
Enantioselective Ni-Catalyzed Electrochemical Synthesis of Biaryl Atropisomers
Chen, Song,Chen, Yue-Gang,Gao, Pei-Sen,Liu, Dong,Ma, Hong-Xing,Mei, Tian-Sheng,Qiu, Hui,Shuai, Bin,Wang, Yun-Zhao
supporting information, p. 9872 - 9878 (2020/06/27)
A scalable enantioselective nickel-catalyzed electrochemical reductive homocoupling of aryl bromides has been developed, affording enantioenriched axially chiral biaryls in good yield under mild conditions using electricity as a reductant in an undivided cell. Common metal reductants such as Mn or Zn powder resulted in significantly lower yields in the absence of electric current under otherwise identical conditions, underscoring the enhanced reactivity provided by the combination of transition metal catalysis and electrochemistry.
