603964-78-9

Basic information

• Product Name: Phosphoramidic dichloride, [[[2-(chloromethyl)phenyl]amino]carbonyl]-
• CAS NO: 603964-78-9
• Molecular Formula: C8H8Cl3N2O2P
• Molecular Weight: 301.496
• Mol File: 603964-78-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phosphoramidic dichloride, [[[2-(chloromethyl)phenyl]amino]carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphoramidic dichloride, [[[2-(chloromethyl)phenyl]amino]carbonyl]-(603964-78-9)
• EPA Substance Registry System: Phosphoramidic dichloride, [[[2-(chloromethyl)phenyl]amino]carbonyl]-(603964-78-9)

Safety Data

• Hazardous Substances Data: 603964-78-9(Hazardous Substances Data)

Upstream product

• 870-30-4 isocyanatophosphonic dichloride 
• 114059-99-3 ortho-(chloromethyl)-aniline 

Relevant articles and documents

Synthesis and antimicrobial activity of N-(substituted)-N′-[1,2,4, 8,10,11-hexachloro-6-oxido-12H-dibenzo(d,g)(1,3,2)-dioxaphosphocin-6-yl]ureas

Substituted dibenzo dioxaphosphocin-6-yl ureas were synthesized by reacting hexachlorophene (4) with different carbamidophosphoric acid dichlorides (3) in the presence of triethylamine in dry toluene at 45-50 °C. Their IR, 1H, 13C and 31P NMR spectral data is discussed. These compounds were found to possess good antimicrobial activity.

Synthesis and antimicrobial activity of 1-[(substituted carbamoyl)amino]-1H,3H-1λ5-[1,3,2]oxazaphospholo[3,4-a] benzimidazol-1-ones

1-[(Substituted carbamoyl)amino]-1H,3H-1λ5-[1,3,2]oxazaphospholo[3, 4-a]benzimidazol-1-ones were synthesized by reacting benzimidazole 2-methanol (4) with different chlorides of carbamidophosphoric acids (3) in the presence of triethylamine at 40-45°C. Th

Synthesis of N-(substituted aryl/cyclohexyl)-N′-[5-bromo-5-nitro-2-oxido-1,3, 2-dioxaphosphorinane-2-yl]ureas

N-(Substituted aryl/cyclohexyl)-N′-[5-bromo-5-nitro-2-oxido-1,3, 2-dioxaphosphorinane-2-yl]ureas RR′P(O)NHC(O)NHR" (5) were synthesized by the reactions of 2-bromo-2-nitro-1,3-propanediol (4) with chlorides of aryl/cyclohexyl carbamidophosphoric acids (3) in the presence of triethylamine at room temperature. Their ir, 1H, 13C and 31P nmr spectral data are discussed.