105-11-3 | 1,4-Benzoquinone dioxime

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$20.00	$14.00
25g	95%	in stock	$23.00	$16.00
100g	95%	in stock	$74.00	$52.00
500g	95%	in stock	$251.00	$176.00

Description

• Catalog Number: AB57424
• Chemical Name: 1,4-Benzoquinone dioxime
• CAS Number: 105-11-3
• Molecular Formula: C6H6N2O2
• Molecular Weight: 138.12404
• MDL Number: MFCD00063636
• SMILES: O/N=C/1\C=C/C(=N/O)/C=C1

Computed Properties

• Complexity: 110
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

p-Benzoquinonedioxime, a versatile compound in chemical synthesis, serves as a valuable tool for various reactions in organic chemistry. Its unique structure and reactivity make it an essential reagent with a wide range of applications.One of the key uses of p-Benzoquinonedioxime is its role as a powerful chelating agent in metal complexation reactions. The oxime groups in the molecule have a high affinity for metal ions, allowing for the formation of stable complexes. This property makes it particularly useful in the purification and separation of metal ions from complex mixtures.In addition, p-Benzoquinonedioxime can also act as a reducing agent in certain chemical transformations. Its ability to undergo redox reactions makes it a valuable reagent for the synthesis of various organic compounds. By selectively reducing functional groups in a molecule, it enables the formation of new chemical bonds and the generation of complex molecular structures.Furthermore, p-Benzoquinonedioxime can participate in cycloaddition reactions, providing a route to the synthesis of heterocyclic compounds. Its reactivity towards dienes and other unsaturated compounds allows for the construction of fused ring systems, which are common motifs in biologically active molecules.Overall, the diverse applications of p-Benzoquinonedioxime in chemical synthesis highlight its importance as a key reagent in modern organic chemistry. Its versatility and unique reactivity make it a valuable tool for researchers and synthetic chemists looking to access new compounds and explore novel reaction pathways.

Literature

• Inter-laboratory evaluation of the bioluminescent Salmonella reverse mutation assay using 10 model chemicals.

  Mutagenesis 20090901

• Mechanistic insight into exclusive nitric oxide recovery from a carbon-bound diazeniumdiolate.

  Nitric oxide : biology and chemistry 20020901