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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,2,4,5-Tetrazine-3,6-diamine

Nc1nnc(nn1)N Request for Quotation
Chemical Name: 1,2,4,5-Tetrazine-3,6-diamine
CAS Number: 19617-90-4
Product Number: AG007R5I(AGN-PC-0JP6SH)
Synonyms:
MDL No:
Molecular Formula: C2H4N6
Molecular Weight: 112.0934

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Chemical Structure


1,2,4,5-Tetrazine-3,6-diamine, commonly known as Tetrazine, is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it a valuable building block in organic chemistry. Tetrazine is predominantly employed in bioconjugation reactions, specifically in the areas of drug development and biomolecule labeling. Due to its rapid and selective reactivity with strained alkenes, Tetrazine is crucial in bioorthogonal chemistry, enabling the efficient conjugation of small molecules to proteins and other biomolecules. Additionally, Tetrazine's utility extends to the preparation of functionalized materials and the synthesis of complex organic molecules. Its compatibility with various functional groups and its high stability under physiological conditions further enhance its applicability in diverse chemical transformations.