78258-13-6

Upstream product

• 51250-39-6 N-(4-nitrophenyl)phosphoramidic dichloride 
• 124-41-4 sodium methylate 
• 67-56-1 methanol 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 86187-30-6 [4-(4-Methyl-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester 
• 90171-98-5 dimethyl N-{4-[(3-amino-9-acridinyl)amino]phenyl}phosphoramidate 
• 86187-25-9 dimethyl N-{4-[(3-nitro-9-acridinyl)amino]phenyl}phosphoramidate 
• 86187-20-4 [4-(3-Methyl-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 90194-65-3 [4-(2-Methyl-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 90171-93-0 [4-(2-Chloro-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 86187-23-7 [4-(3-Bromo-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 86187-21-5 [4-(3-Chloro-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 86187-26-0 [4-(4-Methoxy-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 90171-91-8 [4-(2-Methoxy-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 86187-28-2 [4-(4-Methylcarbamoyl-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 90194-67-5 [4-(3-Methanesulfonyl-acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester; hydrochloride 
• 82720-32-9 [4-(Acridin-9-ylamino)-phenyl]-phosphoramidic acid dimethyl ester 
• 82720-54-5 dimethyl N-(4-aminophenyl)phosphoramidate 

Relevant academic research and scientific papers

Flame retardant cotton fibers produced using novel synthesized halogen-free phosphoramide nanoparticles

Flame retardant cotton fibers were successfully produced using five new nanosized phosphoramide compounds synthesized by ultrasonic method. The 1H NMR spectra of compounds 1-3 illustrate 3J(H,H)cis and 3J(H,H)s

Flame retardant cotton fibers produced using novel synthesized halogen-free phosphoramide nanoparticles

Flame retardant cotton fibers were successfully produced using five new nanosized phosphoramide compounds synthesized by ultrasonic method. The 1H NMR spectra of compounds 1-3 illustrate 3J(H,H)cis and 3J(H,H)s

Certain acridinyl-phosphoramidate compounds

The novel class of compounds of the present invention represented by the general formula (I): STR1 in which R1 represents H or OCH3, R2 represents H, OCH3, CH3, halogen, NO2, NH2, NHCOCH3 or NHCOOCH3, and R3 and R4 individually represent H, CH3, OCH3 or CONHCH3, and the acid addition salts thereof, have unexpectedly high potency and activity in in vivo antitumour tests. The compounds are also bacteriostatic, and show toxicity towards mouse, hamster and human tumour cell lines in culture.

Structural Effects in Amides. Crystal and Molecular Structures of Phosphoric and Carboxylic Anilides

Crystal and molecular structures of three N-aryl carboxylic amides (RCONHAr) and three dimethyl N-arylphosphoramidates (MeO)2P(O)NHAr were determined and are discussed together with those of related systems described in the literature.Carboxylic amides exist in the trans configuration of the CO and NH groups, and both the N-aryl and C-aryl (for R = Ar) rings are considerably twisted with respect to the amide plane.Phosphoramidates prefer the cis orientation of the PO and NH groups, with the N-aryl group bisecting the MeO-P-OMe angle.Substituents in the N-aryl group have a weak effect on structural parameters of both amide functions.For the phosphoramidates a linear free-energy relationship between the intramolecular P=O...H-N hydrogen bonding and the acidity of the ArNH3+ ions has been obtained.