1372810-17-7 Usage
Description
5-(Pentan-3-yl)-1H-tetrazole is an organic compound characterized by its unique tetrazole ring structure with a pentyl group attached to the 5th position. 5-(pentan-3-yl)-1H-tetrazole is known for its potential applications in various chemical and pharmaceutical processes due to its distinct structural features and reactivity.
Uses
Used in Chemical Synthesis:
5-(Pentan-3-yl)-1H-tetrazole is used as a reactant/reagent for the synthetic preparation of sterically stressed constitutional isomers of azaphthalocyanines with fused triazolo rings. Its unique structure allows for the creation of complex and novel molecular architectures that can be further explored for various applications in fields such as materials science, pharmaceuticals, and dyes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(Pentan-3-yl)-1H-tetrazole may be utilized as a building block for the development of new drugs or drug candidates. Its tetrazole ring and pentyl side chain can be exploited to design molecules with specific biological activities, potentially targeting various therapeutic areas.
Used in Dye Industry:
The unique structural features of 5-(Pentan-3-yl)-1H-tetrazole may also make it a valuable component in the development of new dyes with specific color properties and stability. Its use in this industry could lead to the creation of dyes with improved performance characteristics for various applications, such as textiles, plastics, and printing inks.
Check Digit Verification of cas no
The CAS Registry Mumber 1372810-17-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,2,8,1 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1372810-17:
(9*1)+(8*3)+(7*7)+(6*2)+(5*8)+(4*1)+(3*0)+(2*1)+(1*7)=147
147 % 10 = 7
So 1372810-17-7 is a valid CAS Registry Number.
1372810-17-7Relevant articles and documents
Azaphthalocyanines with fused triazolo rings: Formation of sterically stressed constitutional isomers
Novakova, Veronika,Roh, Jaroslav,Gela, Petr,Kunes, Jii,Zimcik, Petr
, p. 4326 - 4328 (2012/05/20)
The presented work deals with synthesis and isolation of constitutional isomers of triazolo-fused azaphthalocyanines. Distribution of the isomers did not follow the statistical calculations due to steric effects of the substituents preferring the least sterically stressed C4h isomer. The Royal Society of Chemistry 2012.
