1660-27-1 Usage
Chemical structure
A benzene ring with two hydroxyl groups and a tetrazole-thioether functional group attached at the 2-position.
Composition
Contains carbon, hydrogen, oxygen, sulfur, and nitrogen atoms.
Molecular weight
Approximately 271.32 g/mol.
Potential applications
Medicinal chemistry, drug development, and organic synthesis.
Interaction with biological targets
Can interact with enzymes and receptors.
Pharmacological activity
May have potential therapeutic effects in the treatment of various diseases.
Research status
Further research and testing are needed to fully understand its properties and potential uses.
Solubility
Information on solubility is not provided in the material.
Stability
Information on stability is not provided in the material.
Reactivity
Information on reactivity is not provided in the material.
Toxicity
Information on toxicity is not provided in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 1660-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1660-27:
(6*1)+(5*6)+(4*6)+(3*0)+(2*2)+(1*7)=71
71 % 10 = 1
So 1660-27-1 is a valid CAS Registry Number.
1660-27-1Relevant articles and documents
Polyfunctional tetrazolic thioethers through electrooxidative/Michael-type sequential reactions of 1,2- and 1,4-dihydroxybenzenes with 1-phenyl-5- mercaptotetrazole
Khodaei, Mohammad M.,Alizadeh, Abdolhamid,Pakravan, Narges
, p. 2527 - 2532 (2008/09/20)
(Chemical Equation Presented) In the presence of 1-phenyl-5- mercaptotetrazole as a nucleophile, electrochemical oxidations of 1,2- and 1,4-dihydroxybenzenes have been investigated in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The voltammetric results indicate that an electrooxidative/Michael-type sequential reaction occurs between the mercaptide anion and the electrochemically generated benzoquinones leading to the corresponding polyfunctional tetrazolic thioethers. The mechanism of electrochemical reaction is proved as an EC pathway using controlled-potential coulometry. In addition, the electrosyntheses of tetrazolic thioethers have been successfully performed in ambient conditions in an undivided cell using an environmentally friendly method with high atom economy.
