60010-56-2 Usage
Uses
Used in Dye Production:
2-(decyloxy)naphthalene is used as a chemical intermediate for the synthesis of dyes, contributing to the coloration and stability of the dyes in different substrates.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(decyloxy)naphthalene serves as a key component in the development of various drugs, potentially due to its ability to interact with biological systems and influence pharmacological properties.
Used as a Solvent:
2-(decyloxy)naphthalene is utilized as a solvent in numerous industrial processes, taking advantage of its solubility properties to dissolve and process other compounds.
Used in Fragrance Industry:
As a fragrance ingredient, 2-(decyloxy)naphthalene is incorporated into perfumes and personal care products, enhancing their scent profiles and providing a unique olfactory experience.
Used in Organic Electronic Materials:
2-(decyloxy)naphthalene finds application in the realm of organic electronics, where its chemical structure and properties are leveraged to improve the performance of electronic devices such as organic light-emitting diodes (OLEDs) and organic solar cells.
Used as a Liquid Crystal Component:
In the field of liquid crystal technology, 2-(decyloxy)naphthalene is employed as a component in liquid crystal mixtures, which are crucial for applications such as display technologies and sensors.
Overall, 2-(decyloxy)naphthalene's versatility and unique characteristics position it as a significant compound across a range of industries, from chemical and pharmaceutical to electronics and personal care.
Check Digit Verification of cas no
The CAS Registry Mumber 60010-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,1 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60010-56:
(7*6)+(6*0)+(5*0)+(4*1)+(3*0)+(2*5)+(1*6)=62
62 % 10 = 2
So 60010-56-2 is a valid CAS Registry Number.
60010-56-2Relevant academic research and scientific papers
Kowtoniuk, Walter E.,MacFarland, Darren K.
, p. 451 - 453 (2005)
Herein we report the cleaving of aryl alkyl ethers on BINOL derivatives, using the common reducing agent LAH. The cleavage of the alkyl oxygen bond is observed when the BINOL derivative is treated with LAH, in refluxing dioxane, for 60 h. The resulting BINOL derivative can then be re-alkylated using a standard Williamson ether synthesis. The same procedure was tested on 6-hydroxy-2-naphthoic acid derivatives and cleavage was not observed, thus suggesting a chelating mechanism for the BINOL ether cleavage.
