1046-56-6 | 3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$22.00	$16.00
5g	98%	in stock	$89.00	$63.00
25g	98%	in stock	$426.00	$298.00
100g	98%	in stock	$1,660.00	$1,162.00

Description

• Catalog Number: AB44241
• Chemical Name: 3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine
• CAS Number: 1046-56-6
• Molecular Formula: C20H14N4
• Molecular Weight: 310.3520
• MDL Number: MFCD00006462
• SMILES: c1ccc(cc1)c1nc(nnc1c1ccccc1)c1ccccn1
• NSC Number: 242686

Computed Properties

• Complexity: 376
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 24
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• XLogP3: 3.1

Upstream Synthesis Route

3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique chemical structure allows for various applications in organic reactions, particularly in the field of heterocyclic chemistry. One of the key applications of 3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine is as a catalyst in organic transformations. Its presence can facilitate the formation of new carbon-carbon or carbon-nitrogen bonds in complex molecules, making it a valuable tool for synthetic chemists. Additionally, this compound can serve as a precursor in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals.Furthermore, 3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine has found use as a fluorescent probe in analytical chemistry. Its fluorescence properties enable its detection and quantification in various chemical and biological samples, making it a valuable tool for researchers studying molecular interactions and reaction mechanisms.In summary, the application of 3-(2-Pyridyl)-5,6-diphenyl-1,2,4-triazine in chemical synthesis spans from catalyzing organic reactions to serving as a fluorescent probe, showcasing its significance in advancing the field of chemistry and its practical relevance in various scientific studies.

Literature

• Di-μ-adipato-κ⁴O¹:O⁶-bis-{aqua-[5,6-di-phenyl-3-(pyridin-2-yl)-1,2,4-triazine-κ²N²,N³]copper(II)}.

  Acta crystallographica. Section E, Structure reports online 20120701

• Di-μ-glutarato-κ(4)O(1):O(5)-bis-{aqua-[5,6-diphenyl-3-(pyridin-2-yl)-1,2,4-triazine-κ(2)N(2),N(3)]copper(II)}.

  Acta crystallographica. Section E, Structure reports online 20120601

• Supercritical carbon dioxide extraction of bioactive compounds from Ampelopsis grossedentata stems: process optimization and antioxidant activity.

  International journal of molecular sciences 20110101

• Dichloridobis(2-chloro-benzyl-κC)[5,6-diphenyl-3-(2-pyrid-yl)-1,2,4-triazine-κN,N]tin(IV).

  Acta crystallographica. Section E, Structure reports online 20090601

• Design of an optical sensor for indirect determination of isoniazid.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080901

• The use of 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine as a precolumn derivatizing reagent in HPLC determination for Fe(II) in natural samples.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20071101

• Ferric and cupric reductase activities by iron-limited cells of the green alga Chlorella kessleri: quantification via oxygen electrode.

  Physiologia plantarum 20071001

• Identification of firearms handling by the [Fe(PDT)(3)](2+) complex: Chemical and time-dependent factors.

  Talanta 20050815

• Identification of firearms holders by the [Fe(PDT)3](+2) complex. Quantitative determination of iron transfer to the hand and its dependence on palmar moisture levels.

  Journal of forensic sciences 20041101

• Amperometric glucose biosensor based on assisted ion transfer through gel-supported microinterfaces.

  Analytical chemistry 20040915

• DNA interactions of cobalt(III) mixed-polypyridyl complexes containing asymmetric ligands.

  Journal of inorganic biochemistry 20040601

• Synthesis, structure, and properties of novel open-cage fullerenes having heteroatom(s) on the rim of the orifice.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20030404

• Development of Zn(II) sensors based on the assisted transfer of metal ions by hydrophobic ligands through gel-supported microinterfaces.

  Fresenius' journal of analytical chemistry 20010401