1848-85-7

Basic information

• Product Name: N-chloro-N'-phenylbenzamidine
• Synonyms: N-chloro-N'-phenylbenzamidine
• CAS NO: 1848-85-7
• Molecular Weight: 230.697
• Mol File: 1848-85-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-chloro-N'-phenylbenzamidine(CAS DataBase Reference)
• NIST Chemistry Reference: N-chloro-N'-phenylbenzamidine(1848-85-7)
• EPA Substance Registry System: N-chloro-N'-phenylbenzamidine(1848-85-7)

Safety Data

• Hazardous Substances Data: 1848-85-7(Hazardous Substances Data)

Upstream product

• 1527-91-9 N²-phenylbenzimidamide 
• 1527-91-9 N-phenylbenzamidine 

Downstream Products

• 5292-05-7 α-(N-phenyl,benzylimino)triphenylphosphorane 
• 94456-90-3 C₁₃H₁₀Cl₃N₂P 
• 120422-01-7 1,4-Dihydro-1,2,4-triphenyl-imidazol-5(H)-one 
• 716-79-0 2-phenyl-1H-benzoimidazole 
• 94456-92-5 C₁₃H₁₁Cl₂N₂OP 
• 77198-19-7 C₂₅H₁₈N₄O₆S 
• 77198-13-1 C₂₃H₂₂N₄O₄S 
• 77198-18-6 C₂₅H₁₈ClN₃O₄S 
• 77198-17-5 C₂₅H₁₉N₃O₄S 
• 77198-16-4 C₂₅H₂₀N₄O₃S 
• 77198-12-0 C₂₃H₂₂ClN₃O₂S 
• 77198-15-3 C₂₅H₂₀ClN₃OS 
• 77198-14-2 C₂₆H₂₃N₃OS 
• 77198-07-3 4-Nitro-N-[1-phenyl-1-phenylamino-meth-(Z)-ylidene]-benzenesulfonamide 

Relevant articles and documents

Experimental and theoretical studies of fused-ring persistent [1,2,4]thiadiazinyl radicals

Five persistent radicals 1a-1e were generated by the oxidation of 4H-[1,2,4]thiadiazines 2a-2e and studied with ESR and UV-vis spectroscopy. Three of the radicals, 1a, 1d, and 1e, were generated in high yields (>90%) using either SO2Cl2/amine in toluene or AgO/K2CO 3 in a toluene/ MeCN mixture. Halogenated radicals 1d and 1e were sufficiently stable for chromatographic isolation and vacuum sublimation. The solution stability of the fluorinated 1d was measured at t1/2 ≈ 4 months in the absence of oxygen, and 1e at t1/2 ≈ 40 min in the presence of air. The crystal and molecular structures of 1d were determined by X-ray crystallography showing columns of parallel almost evenly spaced planar heterocycles connected by infinite ...N...S... chains. Cyclic voltammetry of Id and 1e shows reversible reduction waves at about 0 V and irreversible oxidations at about 1.2 V. Spectral and electrochemical properties of 1 were well reproduced by DFT methods.