17225-95-5 Usage
Uses
Used in Organic Synthesis:
2-naphthalen-2-ylsulfanylethanol is used as a building block in organic synthesis for the creation of various organic molecules. Its structural features make it a versatile component in the construction of complex molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-naphthalen-2-ylsulfanylethanol is utilized as a key intermediate in the development of new drugs. Its ability to form a wide array of derivatives allows for the exploration of potential therapeutic agents.
Used in Asymmetric Synthesis:
2-naphthalen-2-ylsulfanylethanol is used as a chiral auxiliary in asymmetric synthesis. This application is crucial for the production of enantiomerically pure compounds, which is essential in many pharmaceutical and chemical applications where the stereochemistry of a molecule can significantly influence its biological activity and efficacy.
Used in Chemical Production:
2-naphthalen-2-ylsulfanylethanol is used in the production of various chemical products. Its synthesis through the reaction of 2-naphthalenethiol with epichlorohydrin is a key step in the manufacturing process of certain specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 17225-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17225-95:
(7*1)+(6*7)+(5*2)+(4*2)+(3*5)+(2*9)+(1*5)=105
105 % 10 = 5
So 17225-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H12OS/c13-7-8-14-12-6-5-10-3-1-2-4-11(10)9-12/h1-6,9,13H,7-8H2
17225-95-5Relevant academic research and scientific papers
Dynemicin analogs: syntheses, methods of preparation and use
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, (2008/06/13)
A fused ring system compound is disclosed that contains an epoxide group on one side of the fused rings and an enediyne macrocyclic ring on the other side of the fused rings. The compounds have DNA-cleaving, antimicrobial and tumor growth-inhibiting properties. Chimeric compounds having the fused ring system compound as an aglycone bonded to (i) a sugar moiety as the oligosaccharide portion or (ii) a monoclonal antibody or antibody combining site portion thereof that immunoreacts with target tumor cells are also disclosed. Compositions containing a compound or a chimer are disclosed, as are methods of preparing a compound.
Dynemicin analogs: synthesis, methods of preparation and use
-
, (2008/06/13)
A fused ring system compound is disclosed that contains an epoxide group on one side of the fused rings and an enediyne macrocyclic ring on the other side of the fused rings. The compounds have DNA-cleaving, antimicrobial and tumor growth-inhibiting properties. Chimeric compounds having the fused ring system compound as an aglycone bonded to (i) a sugar moiety as the oligosaccharide portion or (ii) a monoclonal antibody or antibody combining site portion thereof that immunoreacts with target tumor cells are also disclosed. Compositions containing a compound or a chimer are disclosed, as are methods of preparing a compound.
