Skip to Content
Merck
All Photos(1)

Documents

403547

Sigma-Aldrich

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

96%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H8N6
CAS Number:
Molecular Weight:
236.23
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

form

solid

mp

225 °C (dec.) (lit.)

SMILES string

c1ccc(nc1)-c2nnc(nn2)-c3ccccn3

InChI

1S/C12H8N6/c1-3-7-13-9(5-1)11-15-17-12(18-16-11)10-6-2-4-8-14-10/h1-8H

InChI key

JFBIRMIEJBPDTQ-UHFFFAOYSA-N

General description

3,6-Di-2-pyridyl-1,2,4,5-tetrazine (DPTZ) undergoes solvothermal reaction with CuSO4.6H2O and Cu(Ac)2.H2O to afford copper containing coordination polymers. It reacts with enamine derivative of morpholine and 5-,6-,7- and 8-membered cyclic ketones to afford pyridazine derivatives.
3,6-Di-2-pyridyl-1,2,4,5-tetrazine undergoes solid-state reaction with fullerene C60 by high-speed vibration milling technique. It acts as electron-deficient diene in the inverse electron demand Diels Alder reaction.

Application

3,6-Di-2-pyridyl-1,2,4,5-tetrazine may be used in the following studies:
  • Preparation of mononuclear, cyclic tetranuclear, and 1-D helical-chain Cu(II) complexes, via metal-assisted hydrolysis.
  • Synthesis of novel cyclic tetranuclear ZnII complex.
  • Synthesis of substituted 3,6-di(2-pyridyl)pyridazines, via inverse electron demand Diels Alder reaction with alkenes or alkynes.

related product

Product No.
Description
Pricing

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and properties of five unexpected copper complexes with ring-cleavage of 3, 6-di-2-pyridyl-1, 2, 4, 5-tetrazine by one pot in situ hydrothermal reaction.
Cui J, et al.
CrystEngComm, 14(6), 2258-2267 (2012)
Synthesis and Characterization of Novel Substituted 3, 6-Di (2-pyridyl) pyridazine Metal-Coordinating Ligands.
Hoogenboom R, et al.
European Journal of Organic Chemistry, 2003(24), 4887-4896 (2003)
Xian-He Bu et al.
Inorganic chemistry, 41(7), 1855-1861 (2002-04-02)
The reactions of 3,6-di-2-pyridyl-1,2,4,5-tetrazine (DPTZ) with different Cu(II) salts generate two new ligands, 2,5-bis(2-pyridyl)-1,3,4-oxodiazole (L(1)) and N,N'-bis(alpha-hydroxyl-2-pyridyl)ketazine (H(2)L(2)), from the metal-assisted hydrolysis of DPTZ, and form three new complexes: a mononuclear complex [Cu(L(1))(2)(H(2)O)(2)] .2ClO(4) (1), a linear coordination polymer [Cu(L(1))(NO(3))(2)](8)
Structure of the Hydration Product of the C60-Di (2-pyridyl)-1, 2, 4, 5-tetrazine Adduct.
Murata Y, et al.
Bulletin of the Chemical Society of Japan, 76(8), 1669-1672 (2003)
Diels-Alder reactions of 3, 6-diphenyl-1, 2, 4, 5-tetrazine and 3, 6-di (2-pyridyl)-1, 2, 4, 5-tetrazine with some 1-morpholinocycloalkenes.
Adnan Atfah M.
Journal of Heterocyclic Chemistry, 26(3), 717-719 (1989)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service