101-38-2 | 2,6-Dichloroquinone-4-chloroimide

Packsize	Purity	Availability	Price	Discounted Price
25g	97%	in stock	$657.00	$460.00

Description

• Catalog Number: AD71170
• Chemical Name: 2,6-Dichloroquinone-4-chloroimide
• CAS Number: 101-38-2
• Molecular Formula: C6H2Cl3NO
• Molecular Weight: 210.44518000000002
• MDL Number: MFCD00001611
• SMILES: Cl/N=C/1\C=C(Cl)C(=O)C(=C1)Cl
• NSC Number: 6293

Computed Properties

• Complexity: 266
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 2.9

Upstream Synthesis Route

2,6-Dichloro-4-(chloroimino)cyclohexa-2,5-dienone, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique chemical structure and reactivity make it a valuable reagent in various organic transformations.One of the key applications of $name$ in chemical synthesis is as a precursor for the synthesis of heterocyclic compounds. By incorporating $name$ into reactions, chemists can introduce specific functional groups and create complex ring systems efficiently. This allows for the synthesis of novel molecules with diverse properties and potential applications in pharmaceuticals, materials science, and agrochemicals.Additionally, $name$ can serve as a key building block in the development of new organic reactions. Its chloroimino moiety provides a reactive site for selective functionalization, enabling the construction of intricate molecular architectures. By leveraging the unique reactivity of $name$, chemists can access new synthetic pathways and streamline the preparation of valuable compounds.Overall, the application of 2,6-Dichloro-4-(chloroimino)cyclohexa-2,5-dienone in chemical synthesis offers a powerful tool for accessing structurally diverse molecules and advancing the field of organic chemistry.

Literature

• In situ synthesis, photometric and spectroscopic studies of chelating system during the 1,4,7,10,13,16-hexaoxacyclooctadecane charge transfer reaction with different acceptors.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20110801

• A cost-effective colorimetric assay for phenolic O-methyltransferases and characterization of caffeate 3-O-methyltransferases from Populus trichocarpa.

  Analytical biochemistry 20090101

• Detection of propranolol in pharmaceutical formulations by diffuse reflectance spectroscopy.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080401

• Electronic, infrared, and 1HNMR spectral studies of the novel charge-transfer complexes of o-tolidine and p-toluidine with alternation pi-acceptors (3,5-dinitro benzoic acid and 2,6-dichloroquinone-4-chloroimide) in CHCl3 solvent.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20060601

• Spectrophotometric stability-indicating methods for the determination of leflunomide in the presence of its degradates.

  Journal of AOAC International 20060101

• [Reactions of iminodibenzyl with 2,6-dichloro-1,4-benzoquinone-4-chlorimide].

  Die Pharmazie 20030301

• Stability indicating methods for assay of mequitazine in presence of its degradate.

  Journal of pharmaceutical and biomedical analysis 20020620

• 2,6-Dichloroquinone chlorimide and 7,7,8,8-tetracyanoquinodimethane reagents for the spectrophotometric determination of salbutamol in pure and dosage forms.

  Journal of pharmaceutical and biomedical analysis 20020615