403547
3,6-Di-2-pyridyl-1,2,4,5-tetrazine
96%
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About This Item
Formula empirica (notazione di Hill):
C12H8N6
Numero CAS:
Peso molecolare:
236.23
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
96%
Stato
solid
Punto di fusione
225 °C (dec.) (lit.)
Stringa SMILE
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
JFBIRMIEJBPDTQ-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
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.
Applicazioni
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.
Prodotti correlati
N° Catalogo
Descrizione
Determinazione del prezzo
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
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)
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)
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)
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)
A spontaneously resolved chiral molecular box: a cyclic tetranuclear ZnII complex with DPTZ (DPTZ= 3, 6-di-2-pyridyl-1, 2, 4, 5-tetrazine).
Bu X, et al.
Chemical Communications (Cambridge, England), 11, 971-972 (2000)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 403547-100G | |
| 403547-1G | 4061831986600 |
| 403547-5G | 4061831986617 |
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