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3,6-Di-2-pyridyl-1,2,4,5-tetrazine, 98%|321216|1671-87-0

3,6-Di-2-pyridyl-1,2,4,5-tetrazine, 98%

Cat. No JK321216_1_G
J&K Chemical

Product Information

Product Name
3,6-Di-2-pyridyl-1,2,4,5-tetrazine, 98%
Brand Name
J&K
Product Number
321216
CAS
1671-87-0
Molecular Formula
C12H8N6
Molecular Weight
236.24
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
315109
IUPAC Name
3,6-dipyridin-2-yl-1,2,4,5-tetrazine
InChI Key
JFBIRMIEJBPDTQ-UHFFFAOYSA-N
SMILES
C1=CC=NC(=C1)C2=NN=C(N=N2)C3=CC=CC=N3

Properties

Melting Point
225

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Dinuclear Radical Tin(IV) Complex Bearing Differently Charged o-Iminoquinone Ligands and Stabilized by a Dianionic Tetrazine Bridge
Publication Name: Journal of Structural Chemistry
Publication Date: 2026-01
DOI: 10.1134/s0022476626010166

Specificity of the reaction between carboryne and 3,6-diaryl-1,2,4,5-tetrazines
Publication Name: Russian Chemical Bulletin
Publication Date: 2025-07
DOI: 10.1007/s11172-025-4696-1

Reactivity Features of ortho-Carboranillithium towards 3,6-Diaryl-1,2,4,5-tetrazines
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2025-06
DOI: 10.1134/s1070428025601578

Interaction of 3,6-Bis(2-pyridyl)-1,2,4,5-tetrazine and 3,4,5,6-Tetrabromo-1,2-dehydrobenzene
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2025-06
DOI: 10.1134/s1070428025602043

Author Correction: Ortho-functionalized pyridinyl-tetrazines break the inverse correlation between click reactivity and cleavage yields in click-to-release chemistry
Publication Name: Communications Chemistry
Publication Date: 2024-12-31
DOI: 10.1038/s42004-024-01392-z|10.1038/s42004-024-01401-1

3,6-Di-2-pyridyl-1,2,4,5-tetrazine, 98%

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