148367-97-9

Basic information

• Product Name: 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE
• Synonyms: 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE;2-Chloro-2-(2-phenylhydrazono)-N-(2-chlorophenyl)-
• CAS NO: 148367-97-9
• Molecular Formula: C14H11Cl2N3O
• Molecular Weight: 308.16
• Mol File: 148367-97-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.33g/cm³
• Refractive Index: 1.62
• PKA: 8.27±0.70(Predicted)
• CAS DataBase Reference: 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE(148367-97-9)
• EPA Substance Registry System: 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE(148367-97-9)

Safety Data

• Hazardous Substances Data: 148367-97-9(Hazardous Substances Data)

Usage

General Description

2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE is a chemical compound with the molecular formula C16H13Cl2N3O. It is a derivative of acetamide and contains chloro and phenyl groups. 2-CHLORO-2-(2-PHENYLHYDRAZONO)-N-(2-CHLOROPHENYL)-ACETAMIDE is a hydrazone derivative, which is a class of organic compounds containing a nitrogen-nitrogen double bond. It is used in organic synthesis and can act as a ligand in coordination chemistry. Its specific properties and uses may vary depending on the context and the specific applications for which it is being used.

InChI:InChI=1/C14H11Cl2N3O/c15-11-8-4-5-9-12(11)17-14(20)13(16)19-18-10-6-2-1-3-7-10/h1-9,18H,(H,17,20)/b19-13+

Upstream product

• 95-51-2 o-chloroaniline 
• 93-70-9 3-oxo-N-2-chlorophenylbutanamide 
• 31009-93-5 2-chloro-N-(2-chlorophenyl)-3-oxobutanamide 
• 62-53-3 aniline 

Relevant articles and documents

Synthesis and structural assignment of oxanilo-N-arylhydrazonoyl chlorides

Oxanilo-N-arylhydrazonoyl chlorides have been prepared from appropriate N-aryl-2-chloro-3-oxobutanamides by the Japp-Klingemann reaction. The structures of the title compounds have been established in the solid state by single-crystal X-ray structure determination and IR spectroscopy, and in solution by IR, UV, and 1H and 13C NMR spectroscopy. The results indicate that the hydrazonoyl chloride moiety adopts the (Z)-configured form. In the crystal, intramolecular hydrogen bonds generally exist between the chloride function and the hydrazone hydrogen atom, and also between the amide hydrogen atom and the double-bonded nitrogen atom of the hydrazone moiety. In solution, this intramolecular hydrogen bonding could not be detected. In compounds with an ortho-chloro-substituted NH-aryl moiety, however, the chlorine atom is involved in hydrogen bonding to the NH hydrogen atom both in the crystal and in solution. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.