TCI B7003 1-(tert-Butyl)-3-(methylthio)-5-phenyl-1,2,4-triazin-1-ium trifluoromethanesulfonate is a cationic triazinium reagent developed for conjugation chemistry. The electron-poor triazinium ring is designed for inverse electron demand Diels–Alder reactions, a widely used bioorthogonal ligation strategy. Its tert-butyl, methylthio, and phenyl substituents tune both the steric environment and the electronic character of the ring. AMI Scientific supplies this chemical biology reagent in 200 mg and 1 g pack sizes.
Related TCI products
- TCI A3817 3-[4-(Ammoniomethyl)phenyl]-1-(tert-butyl)-5-phenyl-1,2,4-triazin-1-ium Ditrifluoromethanesulfonate
- TCI M4025 28735-27-5 3-(Methylthio)-5-phenyl-1,2,4-triazine
- TCI D6289 293311-03-2 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium Tetrafluoroborate
- TCI D2919 3945-69-5 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride
- TCI A3543 1120-99-6 1,2,4-Triazin-3-amine
- TCI A3095 933-20-0 4,6-Dichloro-1,3,5-triazin-2-amine
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- Kisliy et al. (2004). 4‐Amino‐6‐(tert‐butyl)‐3‐methylthio‐4,5‐dihydro‐1,2,4‐triazin‐5‐one in Nucleophilic Substitution Reactions with Carboxylic Acid Hydrazides.. ChemInform doi:10.1002/chin.200415152
- Kisliy et al. (2003). 4-Amino-6-(tert-butyl)-3-methylthio-4,5-dihydro-1,2,4-triazin-5-one in Nucleophilic Substitution Reactions with Carboxylic Acid Hydrazides. Chemistry of Heterocyclic Compounds doi:10.1023/a:1025623902326
- Kodama et al. (2021). 4,4′-Di-tert-butyl-2,2′-bipyridinium Trifluoromethanesulfonate. Molbank doi:10.3390/m1261
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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- Pharmaceutical Development and Drug Discovery ResearchAlbumin Binding AgentsAlbumin Binding Modification Reagents
- Pharmaceutical Development and Drug Discovery ResearchBioconjugationCopper-free Click Reaction Reagents
- Pharmaceutical Development and Drug Discovery ResearchBioconjugationAlbumin Binding Modification Reagents
- Pharmaceutical Development and Drug Discovery ResearchConjugation Chemistry/Click ChemistryCopper-free Click Reaction Reagents

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