875-83-2 Usage
Description
Sodium 2-naphtholate, also known as sodium beta-naphtholate, is a sodium salt of 2-naphthol, a white to light yellow crystalline solid that is soluble in polar solvents such as water and ethanol. It is a chemical compound commonly used as a reagent in organic synthesis and as a catalyst in various chemical reactions.
Uses
Used in Organic Synthesis:
Sodium 2-naphtholate is used as a reagent for the synthesis of dyes, pharmaceuticals, and other organic compounds due to its versatile nature and reactivity.
Used in Chemical Reactions:
Sodium 2-naphtholate is used as a catalyst in various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used as a Deprotonating Agent:
Sodium 2-naphtholate is used as a deprotonating agent in organic reactions, facilitating the transfer of protons and promoting the formation of desired products.
Used as a Mediator in Oxidation Reactions:
Sodium 2-naphtholate is used as a mediator in the oxidation of organic compounds, enabling controlled and selective oxidation processes.
Used in Chemical Research:
Sodium 2-naphtholate is a valuable tool in organic chemistry and chemical research, contributing to the development of new synthetic methods and the understanding of reaction mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 875-83-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 875-83:
(5*8)+(4*7)+(3*5)+(2*8)+(1*3)=102
102 % 10 = 2
So 875-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O.Na/c11-10-6-5-8-3-1-2-4-9(8)7-10;/h1-7,11H;/q;+1/p-1
875-83-2Relevant articles and documents
Feasible Approach to Tricyclic and Tetracyclic cyclododecanone
Zoorob, Hanafi H.,Elsherbini, Mohamed S.,Hamama, Wafaa S.
, p. 941 - 944 (2016/05/19)
2-Bromocyclododecanone was utilized as precursor to synthesize polyfused heterocyclic cyclododecane ring systems. Transformation of 2-bromocyclododecanone (5) with 1H-benzimidazole-2-thiole (6), benzo[d]thiazole-2-thiol (9), 2-naphthol (12), and thiophenol (15) afforded thiazolo[2,3-b]benzimidazole (8), thiazolo[2,3-b]benzothaizole derivative (11) naphtho[1,2-d]furan derivative (14) and 2-(phenylthio)cyclododecanone (16), respectively.
VIRAL POLYMERASE INHIBITORS
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Page/Page column 97, (2009/04/25)
Compound of Formula I: wherein, R2, R5 and R6 are defined herein, are useful as inhibitors of the hepatitis C virus NS5B polymerase
Process for dehydrating hydrous sodium Beta-naphtholate
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Page/Page column 4; 5, (2010/02/10)
The present invention provides a process for dehydrating hydrous sodium β-naphtholate comprising: the step of heating the hydrous sodium β-naphtholate or a mixture of the hydrous sodium β-naphtholate and β-naphthol which comprises no more than 0.2 mole of β-naphthol per one mole of sodium β-naphtholate in a solvent at a temperature of 260-300°C under an inert gas. The process makes it possible to dehydrate hydrous sodium β-naphtholate thoroughly in a short time with less production of tarry components.