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Pyrazine-2-amidoxime Sale

(Synonyms: 吡嗪-2-甲胺肟) 目录号 : GC44783

A synthetic intermediate useful for pharmaceutical synthesis

Pyrazine-2-amidoxime Chemical Structure

Cas No.:51285-05-3

规格 价格 库存 购买数量
500mg
¥361.00
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1g
¥686.00
现货
5g
¥2,912.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Pyrazine-2-amidoxime is a synthetic intermediate useful for pharmaceutical synthesis.

Chemical Properties

Cas No. 51285-05-3 SDF
别名 吡嗪-2-甲胺肟
Canonical SMILES N/C(C1=NC=CN=C1)=N\O
分子式 C5H6N4O 分子量 138.1
溶解度 DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 0.2 mg/ml,PBS (pH 7.2): 0.1 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 7.2411 mL 36.2056 mL 72.4113 mL
5 mM 1.4482 mL 7.2411 mL 14.4823 mL
10 mM 0.7241 mL 3.6206 mL 7.2411 mL
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Research Update

Pyrazine-2-amidoxime Ni(II) complexes: from ferromagnetic cluster to antiferromagnetic layer

Inorg Chem 2011 Feb 7;50(3):1079-83.PMID:21175167DOI:10.1021/ic1022714.

Tetranuclear [Ni(4)(Hpzaox)(2)(pzaox)(2)(py)(4)](ClO(4))(2)·2py (1), [Ni(4)(Hpzaox)(2)(pzaox)(2)(py)(4)](NO(3))(2)·4py (2), and two-dimensional (2D) [Ni(4)(Hpzaox)(2)(pzaox)(2)(H(2)O)(2)](NO(3))(2)·2H(2)O (3) are prepared via the reaction of NiX(2)·6H(2)O and Pyrazine-2-amidoxime (H(2)pzaox). All compounds contain [Ni(4)(Hpzaox)(2)(pzaox)(2)](2+) fragments, which assemble to form a tetranuclear or polymeric network. Magnetic studies show that the tetranuclear compounds display usual ferromagnetic coupling via the oxime N-O bridges, and the 2D compound displays unusual antiferromagnetic behavior.

High-nuclear heterometallic oxime clusters assembled from triangular subunits: solvothermal syntheses, crystal structures and magnetic properties

Dalton Trans 2017 Dec 19;47(1):169-179.PMID:29192927DOI:10.1039/c7dt03692b.

Three series of six Pyrazine-2-amidoxime (H2pzaox)-based 3d-4f clusters, {Ln8Ni6}, {Ln5Ni10} and {Ln5Ni8} (Ln = Dy and Gd), were solvothermally synthesized in the absence or presence of different coligands, and were structurally and magnetically characterized. The unusual ring-shaped {Ln8(μ3-OH)4} core in the two {Ln8Ni6} complexes is generated by four corner-sharing triangle {Ln3(μ3-OH)} units, which are further connected to six outer NiII ions by twelve deprotonated H2pzaox ligands in three common binding modes. By contrast, the remaining four clusters contain only two corner-sharing {Ln3(μ3-OH)} triangles, which interact with peripheral NiII ions through fourteen H2pzaox ligands in five (for {Ln5Ni10}) and four (for {Ln5Ni8}) different bridging ways. Thus, the interesting core motifs observed in these clusters depend significantly on the number of the triangular {Ln3(μ3-OH)} subunits and their connectivity manner with the singly and doubly deprotonated Pyrazine-2-amidoxime ligand. Additionally, weak ferromagnetic superexchange in the {Dy5Ni10} and {Ln5Ni8} clusters and antiferromagnetic coupling in {Ln8Ni6} and {Gd5Ni10} clusters was respectively mediated by versatile oximate bridges between the intramolecular LnIII and NiII ions. Furthermore, the three DyIII-derived aggregates exhibit slightly temperature-dependent magnetic relaxations under a zero dc field, and the three GdIII-based clusters display large magnetic entropy changes of 23.5 J kg-1 K-1 for {Gd8Ni6}, 19.4 J kg-1 K-1 for {Gd5Ni10}, and 22.4 J kg-1 K-1 for {Ln5Ni8} at 4.0 K and 70 kOe. These interesting results are helpful for the understanding of oximate-based 3d-4f coordination chemistry and their structure-function relationships.