93356-05-9 Usage
Chemical class
Tetrazine derivatives
Applications
Pharmaceuticals
Materials science
Bioconjugation
Reactivity
Unique and efficient in bioorthogonal reactions
Importance
Valuable tool for chemical biology and drug discovery research
Structure
Tetrazine ring
Two naphthalene sulfonyl substituents
Two methylphenyl substituents
Properties and reactivity
Influenced by the presence of naphthalene sulfonyl and methylphenyl groups
Scientific and industrial significance
Diverse applications in various fields
These properties and specific content provide a comprehensive overview of 1,2,4,5-Tetrazine, 1,4-dihydro-3,6-bis(4-methylphenyl)-1,4-bis(2-naphthalenylsulfonyl)-, highlighting its importance in the fields of pharmaceuticals, materials science, and bioconjugation.
Check Digit Verification of cas no
The CAS Registry Mumber 93356-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,5 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93356-05:
(7*9)+(6*3)+(5*3)+(4*5)+(3*6)+(2*0)+(1*5)=139
139 % 10 = 9
So 93356-05-9 is a valid CAS Registry Number.
93356-05-9Relevant academic research and scientific papers
Synthesis of Some Triazole, Tetrazole, and Tetrazine Derivatives from N-β-Naphthalenesulfonylbenzohydrazidoyl Chlorides
Hassaneen, Hamdi M.,Fahmi, Abdelgawad A.,Abdelhamid, Hyam,Yassin, Ahmady A.,Shawali, Ahmad S.
, p. 797 - 800 (2007/10/02)
A series of N-β-naphthalenesulfonylbenzohydrazidoyl chlorides 8a-d has been prepared by the action of thionyl chloride on the corresponding hydrazides 7a-d.Treatment of 8 with triethylamine and morpholine afforded the tetrazines 10 and the amidrazones 11 respectively.Acid hydrolysis of 11 yielded the hydrazides 7.Reaction of 8 with phenylhydrazine gave 3,5-diaryltetrazoles 14.However, reaction of 8 with aroylhydrazines yielded 3,5-diaryl-4-β-naphthalenesulfonylamino-4H-1,2,4-triazoles 15.The structures of the products were assigned upon the basis of their spectra, elemental analyses and alternative synthesis whereever possible.
