59020-06-3 Usage
Uses
Trimethyl(4-pyridyl)tin is used in various applications across different industries, primarily due to its unique chemical properties and reactivity. Some of the known uses include:
Used in Chemical Research:
Trimethyl(4-pyridyl)tin is used as a research compound for studying the properties and reactivity of organotin compounds. Its unique structure and chemical bonds make it an interesting subject for scientific investigation.
Used in Pharmaceutical Industry:
Trimethyl(4-pyridyl)tin is used as a potential therapeutic agent in the development of new drugs. Its organotin nature may offer novel pharmacological properties that could be harnessed for medical applications.
Used in Material Science:
Trimethyl(4-pyridyl)tin is used as a component in the synthesis of new materials with unique properties. Its organotin structure may contribute to the development of advanced materials with potential applications in various fields.
Used in Environmental Applications:
Trimethyl(4-pyridyl)tin is used as a catalyst or additive in environmental remediation processes. Its reactivity may enable the development of new methods for pollution control and waste management.
Check Digit Verification of cas no
The CAS Registry Mumber 59020-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,2 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59020-06:
(7*5)+(6*9)+(5*0)+(4*2)+(3*0)+(2*0)+(1*6)=103
103 % 10 = 3
So 59020-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N.3CH3.Sn/c1-2-4-6-5-3-1;;;;/h2-5H;3*1H3;/rC8H13NSn/c1-10(2,3)8-4-6-9-7-5-8/h4-7H,1-3H3
59020-06-3Relevant articles and documents
Heterocyclic substituted-phenoxyalkylisoxazoles as antiviral useful agents
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, (2008/06/13)
Compounds of the formula STR1 wherein: Y is an alkylene bridge of 3-9 carbon atoms; Z is N or HC; R is hydrogen or lower-alkyl of 1-5 carbon atoms, with the proviso that when Z is N, R is lower-alkyl; R1 and R2 are hydrogen, halogen, lower-alkyl, lower-alkoxy, nitro, lower-alkoxycarbonyl or trifluoromethyl; and Het is selected from specified heterocyclic groups, are useful and antiviral agents, particularly against picornaviruses, including numerous strains of rhinovirus.