7598-29-0 Usage
Uses
Used in Organic Synthesis:
3-(naphthalen-2-yloxy)propan-1-ol is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, leveraging its unique chemical structure and reactivity to create novel compounds with potential therapeutic or agricultural applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(naphthalen-2-yloxy)propan-1-ol is utilized as a key intermediate in the development of new drugs, owing to its potential to contribute to the design of molecules with specific biological activities and therapeutic effects.
Used in Material Science and Engineering:
3-(naphthalen-2-yloxy)propan-1-ol may have potential uses in material science and engineering, where it can be employed to modify the physical and chemical properties of polymers and other materials, enhancing their performance in various applications.
While the specific applications and properties of 3-(naphthalen-2-yloxy)propan-1-ol have not been extensively studied, its unique structure suggests a broad range of possible uses across different industries, particularly in the development of innovative pharmaceuticals, agrochemicals, and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 7598-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7598-29:
(6*7)+(5*5)+(4*9)+(3*8)+(2*2)+(1*9)=140
140 % 10 = 0
So 7598-29-0 is a valid CAS Registry Number.
7598-29-0Relevant academic research and scientific papers
Nucleophilic Hydroxylation in Water Media Promoted by a Hexa-Ethylene Glycol-Bridged Dicationic Ionic Liquid
Jadhav, Vinod H.,Kim, Jin Gwan,Jeong, Hyeon Jin,Kim, Dong Wook
, p. 7275 - 7280 (2015/07/28)
Hexaethylene glycol bis(3-hexaethylene glycol imidazolium) dimesylate ionic liquid (hexaEG-DHIM) was designed and prepared as a highly efficient promoter for the nucleophilic hydroxylation of alkyl halides to the corresponding alcohol products in neat water media. It was observed that hexaEG-DHIM promoter enhanced the nucleophilicity of water significantly in the reaction. In addition, the hexaEG-DHIM could be reused several times without loss of activity. Moreover, the hydroxylation reactions of base-sensitive and/or polar alkyl halide substrates proceeded highly chemoselectively in excellent yields.
