53662-42-3 Usage
Molecular weight
161.22 g/mol
Type of compound
Tetrazole derivative with a thiol group
Common uses
Reagent in organic synthesis and pharmaceutical research
Potential applications
Drug discovery and development, acting as a ligand for metal ions, and pharmacological properties
Unique features
Important building block in the synthesis of various biologically active molecules and materials
Studied activities
Anti-inflammatory, antioxidant, and antimicrobial.
Check Digit Verification of cas no
The CAS Registry Mumber 53662-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53662-42:
(7*5)+(6*3)+(5*6)+(4*6)+(3*2)+(2*4)+(1*2)=123
123 % 10 = 3
So 53662-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N4S/c1-6-4-2-3-5-7(6)12-8(13)9-10-11-12/h2-5H,1H3,(H,9,11,13)
53662-42-3Relevant academic research and scientific papers
Product and preparation of 1H-tetrazole-5-thiol derivatives
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, (2008/06/13)
The process for preparation of and the intermediate compounds such as 1H-tetrazole-5-thiol having the formula STR1 wherein R1 is alkyl, aminoalkyl, acylaminoalkyl, aryl, alkoxycarbonylaminoalkyl, halogen-substituted aryl or alkylamino-substituted aryl and R2 is hydrogen or arakyl, preferably benzyl. The compound is produced by reacting a substituted thiosemicarbazide with an aralkyl chloride, subjecting the resultant compound to diazotization, and reacting the resultant compound with a Friedel Crafts catalyst. Optionally, this may be further hydrolyzed when R1 is aminoalkyl and/or converted to conventional salts.
