14817-38-0 Usage
Description
2-(prop-2-yn-1-yloxy)phenol, also known as propargylphenol, is a phenolic compound characterized by the molecular formula C9H8O2. It features a propargylic ether functional group attached to a phenol moiety, which endows it with unique chemical properties. 2-(prop-2-yn-1-yloxy)phenol is utilized as a versatile building block in the synthesis of more complex organic molecules and has garnered interest for its potential applications as an antioxidant and antimicrobial agent. Its distinctive chemical structure also positions it as a promising candidate in biomedical and pharmaceutical research. However, due to potential hazards to human health and the environment, careful handling and management of propargylphenol are essential.
Uses
Used in Organic Synthesis:
2-(prop-2-yn-1-yloxy)phenol is used as a building block in the synthesis of more complex organic compounds for various applications across different industries. Its propargylic ether functional group allows for a wide range of chemical reactions, making it a valuable intermediate in organic chemistry.
Used in Antioxidant Applications:
2-(prop-2-yn-1-yloxy)phenol is used as an antioxidant in various industrial processes. Its phenolic structure provides it with the ability to scavenge free radicals, thereby preventing oxidative damage and extending the shelf life of products in which it is used.
Used in Antimicrobial Applications:
2-(prop-2-yn-1-yloxy)phenol is used as an antimicrobial agent in different settings, such as in the formulation of disinfectants and preservatives. Its ability to inhibit the growth of microorganisms makes it a useful component in products that require protection against microbial contamination.
Used in Biomedical and Pharmaceutical Research:
2-(prop-2-yn-1-yloxy)phenol is used as a research compound in the biomedical and pharmaceutical fields. Its unique chemical structure offers potential for the development of new drugs and therapeutic agents, particularly in areas where its antioxidant and antimicrobial properties could be beneficial.
Used in Environmental Management:
2-(prop-2-yn-1-yloxy)phenol is used in environmental management strategies to mitigate the impact of hazardous substances. Its chemical properties may allow it to be employed in processes that neutralize or break down harmful compounds, thus contributing to a cleaner and safer environment.
Check Digit Verification of cas no
The CAS Registry Mumber 14817-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,1 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14817-38:
(7*1)+(6*4)+(5*8)+(4*1)+(3*7)+(2*3)+(1*8)=110
110 % 10 = 0
So 14817-38-0 is a valid CAS Registry Number.
14817-38-0Relevant articles and documents
Design, Synthesis, and Evaluation of Novel L-Pyroglutamic Acid Derivatives as Potent Antifungal Agents
Sun, Mingxia,Han, Lijuan,Li, Aijuan,Zhu, Xunzhen,Wu, Wenjun,Zhang, Jiwen
, p. 1081 - 1085 (2021/11/22)
A series of novel L-pyroglutamate containing 1,2,3-triazole ring substructures was synthesized and characterized by adopting an appropriate synthetic scheme. The effect of different substituents on the triazole ring at the ortho-, meta- and para-positions
Syntheses and structures of isomeric [6.6]- and [8.8]cyclophanes with 1,4-dioxabut-2-yne and 1,6-dioxahexa-2,4-diyne bridges
Srinivasan,Sankararaman,Hopf,Dix,Jones
, p. 4299 - 4303 (2007/10/03)
All three isomers (ortho, meta, and para) of [8.8] cyclophane bearing 1,6-dioxahexa-2,4-diyne bridges have been synthesized and structually characterized by single-crystal X-ray crystallography to determine the conformation of the cyclophanes and their cavity dimensions. The three isomeric [6.6]cyclophanes bearing 1,4-dioxabut-2-yne bridges have also been synthesized from but-2-yne-1,4-diol ditosylate and the isomeric dihydroxybenzenes. The [6.6]orthocyclophane has been structurally characterized by single-crystal X-ray crystallography. The energy-minimized structures from the semiempirical AM1 calculations of these cyclophanes compare very well with the structures obtained by X-ray crystallography.
