5432-97-3 Usage
Description
1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is a chemical compound with the molecular formula C20H14OS. It is a naphthalene derivative that features a naphthalene ring with a thiol (sulfanyl) group attached to it, as well as a hydroxyl group at the 2-position. 1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is known for its versatile reactivity due to the presence of both a thiol and a hydroxyl group in its structure, making it a valuable building block in organic synthesis and research.
Uses
Used in Organic Synthesis:
1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is used as a building block in organic synthesis for the preparation of various organic compounds. Its unique structure with a thiol and hydroxyl group allows for a wide range of chemical reactions, contributing to the diversity of synthesized products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is used as a precursor for the development of new drugs. Its versatile reactivity and structural features make it a promising candidate for creating novel therapeutic agents.
Used in Research:
1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is also utilized in research settings to study its chemical properties and potential applications. 1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol's reactivity and structural characteristics provide valuable insights for scientists working on the development of new materials and drug candidates.
Used in the Synthesis of Functional Materials:
1-(naphthalen-2-ylsulfanyl)naphthalen-2-ol is used as a precursor in the synthesis of various functional materials. The presence of both a thiol and a hydroxyl group in its structure makes it a valuable component in the creation of materials with specific properties for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5432-97-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5432-97:
(6*5)+(5*4)+(4*3)+(3*2)+(2*9)+(1*7)=93
93 % 10 = 3
So 5432-97-3 is a valid CAS Registry Number.
5432-97-3Relevant articles and documents
An alternative synthetic path to 1-substituted 2-naphthol
Blanco, Guillermo Aldo,Baumgartner, Maria Teresa
, p. 2306 - 2309 (2010)
The photoinduced substitution of the 2-naphthoxide anion was carried out using diethylphosphite, benzenethiolate or 2-naphthalenethiolate anions in the presence of an electron acceptor. The corresponding products were afforded in good yield. This is a sim
Aerobic Cross-Dehydrogenative Coupling Reactions for Selective Mono- And Dithiolation of Phenols
Han, Dong-Yang,Liu, Xiao-Peng,Li, Ruo-Pu,Xu, Da-Zhen
, p. 10166 - 10176 (2021/07/31)
A highly efficient strategy for the direct thiolation of phenols under transition metal-free and solvent-free conditions has been developed. These reactions are operationally simple with employing air (molecular oxygen) as an ideal oxidant and can selectively provide mono- and dithiolation products in good to excellent yields under basic conditions. The reaction tolerates a broad range of aryl thiols and arenes and is especially applicable for large-scale synthesis.
Metal free, facile sulfenylation of ketene dithioacetals catalyzed by an HBr-DMSO system
Sorabad, Ganesh Shivayogappa,Maddani, Mahagundappa Rachappa
supporting information, p. 5996 - 6000 (2019/04/16)
A transition metal free, highly efficient, sulfenylation of ketene dithioacetals catalyzed by an HBr-DMSO system is achieved. This strategy employs inexpensive and readily available HBr and DMSO to provide a direct C-H bond sulfenylation with a broad rang
