17225-95-5 Usage
General Description
2-naphthalen-2-ylsulfanylethanol is a chemical compound with a molecular formula C12H12OS. It is also known as 2-(2-naphthylthio)ethanol and is a thiol compound with a naphthalene ring. 2-naphthalen-2-ylsulfanylethanol is used in organic synthesis and pharmaceutical research as a building block for various organic molecules. It can be synthesized through the reaction of 2-naphthalenethiol with epichlorohydrin, and it can undergo further reactions to produce different derivatives. 2-naphthalen-2-ylsulfanylethanol is also used as a chiral auxiliary in asymmetric synthesis, making it a valuable compound in the field of organic chemistry.
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 articles and documents
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.
