626-37-9

Usage

InChI:InChI=1/C3H6N2O4/c1-2-9-3(6)4-5(7)8/h2H2,1H3,(H-,4,6,7,8)/p+1

Upstream product

• 64-17-5 ethanol 
• 62261-13-6 silver N-nitroethylcarbamate 
• 74-88-4 methyl iodide 
• 141972-53-4 S,S-dimethyl N-(nitro)imidodithiocarbonate 
• 176501-96-5 N,N′-dinitrourea 
• 7791-25-5 sulfuryl dichloride 
• 80284-09-9 nitro-carbamic acid ethyl ester; potassium salt 
• 71-43-2 benzene 
• 22012-90-4 nitrosourethane 
• 64-19-7 acetic acid 
• 7664-93-9 sulfuric acid 
• 7697-37-2 nitric acid 
• 51-79-6 urethane 
• 7601-90-3 perchloric acid 

Downstream Products

• 19199-80-5 nitro-(1-phenyl-ethyl)-amine 
• 4114-31-2 ethylhydrazine carboxylate 
• 91-01-0 1,1-Diphenylmethanol 
• 52917-30-3 N,N'-Dibenzyl-N-aethoxycarbonylharnstoff 
• 101-99-5 N-carboethoxyaniline 
• 1027646-36-1 N-Ethoxycarbonyl-1-(4'-isobutylphenyl)-1-nitroamino-ethan 
• 7697-37-2 nitric acid 
• 51-79-6 urethane 
• 49679-15-4 N-carbobenzyloxyurea 

Relevant academic research and scientific papers

Nitrimines: VII. Reaction of S,S′-Dimethyl-N-nitroimidodithiocarbonate with Alkali. Synthesis of S-Methyl-N-nitrothiocarbamate and Its Salts

Reaction of S,S′-dimethyl-N-nitroimidodithiocarbonate with alkali in aqueous-alcoholic solution results in salts of S-methyl-N-nitrothiocarbamate. In anhydrous ethanol a salt of nitrouretane is obtained. By the reaction of S-methyl-N-nitrothiocarbamate salts with hydrazine 4-nitrosemicarbazide salts were prepared.

Dinitramide and its salts 10. * synthesis of dinitramide salts from N,N-dinitro derivatives of organic amides

N,N-Dinitro derivatives of alkylurethanes, benzamide, and p-toluenesulfamide were synthesized for the first time. Their reactions with ammonia afforded the ammonium salt of dinitramide in 44-85 % yields.

Chemistry of urea nitro derivatives: III. Reactions of N,N′ -dinitrourea with bases

N,N′-Dinitrourea reacts with bases to form the corresponding acid or neutral salts. Its reaction with hydrazine yields 4-nitrosemicarbazide, and the reaction with hydroxylamine leads to N-hydroxy-N′-nitrourea.

Activation of nitrogen bronsted acids: Synthesis and reactivity of a new class of nitrogen acid complexes

The nitrogen acids RC(O)NHNO2, N-nitroamide, R = CH3 (1), C2H5 (2) and N-nitrocarbamate, R′OC(O)NHNO2, R′ = CH3 (3), C2H5 (4) are a class of primary N-nitrocarboxamide compounds that oxidatively add to trans-Ir(I)(Cl)(N2)(PPh3)2 to give six-coordinate Ir(III)(η2-(NO2)-nitrogen acid)(H)(Cl)(PPh3)2 complexes 5-8. Unexpected fluxional behavior of the complexes in solution is observed by 1H NMR spectroscopy. Reaction intermediates of the oxidative addition reactions were also observed and monitored using 31P and 1H NMR and solution IR spectroscopies. Complex 5 reacts with methyl triflate in CH3CN to generate bis(acetonitrile) complex (9) from a net loss of the nitrogen acid anion. P(CH3)2Ph reacts with 5 to give phosphine-substituted and P(CH3)2Ph addition isomers (10). Reactivity studies of 5 with CO gave metastable CO adduct isomer 11, which loses CO on prolonged standing in solution. (Chemical Equation Presented).

Chemistry of urea nitro derivatives: II. Synthesis of nitramide from N,N′-dinitrourea. New reactions of nitramide

Study of the hydrolysis of N,N′-dinitrourea resulted in the development of convenient procedures for synthesizing nitramide on the basis of urea. New reactions of nitramide were examined.

Process for producing an aromatic urethane

An aromatic urethane is obtained at high yield without involving corrosion of a stainless steel reactor by interacting an aromatic nitro compound, an organic compound having at least one hydroxyl group therein and carbon monoxide in the presence of a cata