Thiamphenicol aminoacetate hydrochloride

Application N -(2-hydroxyethyl)ethylenediamine (hydeten) or [ N -(2-aminoethyl)ethanolamine] can be used as: A precursor in the synthesis of room-temperature ionic liquids, acetate and formate ammonium salts of N -(2-hydroxyethyl)-ethylenediamine.

Other Notes Mono-protected derivative of ethylenediamine, preparation of pharmacologically active analogues introduction of an ethylenediamine spacer.

Other Notes Mono-protected derivative of ethylenediamine, preparation of pharmacologically active analogues introduction of an ethylenediamine spacer.

Other Notes Mono-protected derivative of ethylenediamine, preparation of pharmacologically active analogues introduction of an ethylenediamine spacer.

Application N -Boc- m -phenylenediamine ( tert -Butyl-3-aminophenylcarbamate) may be used in the preparation of: 5,5&#8242-(propane-2,2-diyl)bis( N -(3-aminophenyl)-4-methyl-3-phenyl-1 H -pyrrole-2-carboxamide) ethyl 4-[{3-[( tert

N-Ethylethylenediamine undergoes condensation with 2-hydroxy-3-methoxybenzaldehyde . It also forms organometallic ruthenium(II) complexes that inhibit the growth in human ovarian cancer cell lines .

N -Methyl-1,2-phenylenediamine is an ortho -diamine. In situ generated diazonium cations of N -methyl-1,2-phenylenediamine were used for the electrochemical modification of glassy carbon electrode.

N -Methyl-1,2-phenylenediamine is an ortho -diamine. In situ generated diazonium cations of N -methyl-1,2-phenylenediamine were used for the electrochemical modification of glassy carbon electrode.

N-Methylethylenediamine undergoes condensation with pyridine-2-carboxaldehyde to form an imine . It reacts with isoquinoline-5-sulfonyl chloride to form N-(2-aminoethyl)-N-methyl-isoquinoline-5-sulfonamide .

N-Methylethylenediamine undergoes condensation with pyridine-2-carboxaldehyde to form an imine . It reacts with isoquinoline-5-sulfonyl chloride to form N-(2-aminoethyl)-N-methyl-isoquinoline-5-sulfonamide .

N-Methylethylenediamine undergoes condensation with pyridine-2-carboxaldehyde to form an imine . It reacts with isoquinoline-5-sulfonyl chloride to form N-(2-aminoethyl)-N-methyl-isoquinoline-5-sulfonamide .

N-Tosylethylenediamine