CAS No.598-57-2,N-nitromethylamine Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

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Qingdao Beluga Import and Export Co., LTD

N-nitromethylamine CAS:598-57-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermed

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Shandong Hanjiang Chemical Co., Ltd.

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

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Zibo Hangyu Biotechnology Development Co., Ltd

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Hangzhou J&H Chemical Co., Ltd.

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Xian Changyue Biological Technology Co., Ltd.

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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DB BIOTECH CO., LTD

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N-nitromethylamine

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Hangzhou Fandachem Co.,Ltd

Methanamine, N-nitro-(9CI) cas 598-57-2Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

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Henan Kanbei Chemical Co.,LTD

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Shanghai Chinqesen Biotechnology Co., Ltd.

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Hebei Muhuang Technology Co., Ltd

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ZHEJIANG JIUZHOU CHEM CO.,LTD

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HuBei Ipure Biotech CO.,ltd

HuBei ipure is a diversified product production and operation enterprise, with API, pharma intermediates, and other fine chemicals as well as R&D and pigments development and sales as one of the large enterprises, with more than 130 acres of pl

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Nanjing Raymon Biotech Co., Ltd.

Methanamine, N-nitro-(9CI)Appearance:Off white to slight yellow solid Storage:keep in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/pharma intermediate Transportation:By Sea,by Air,By courier like

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Synthetic route

: 96-31-1
N,N'-Dimethylurea

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
Stage #1: N,N'-Dimethylurea With sulfuric acid; nitric acid In dichloromethane at -5 - 0℃; Stage #2: In water at 20℃; for 1h; Temperature;	89.2%

: 141-52-6
sodium ethanolate

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

A: 36234-10-3
3-Oxo-3-phenylpropanal 1-(diethylacetal)

B: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
In ethanol at 35 - 40℃; for 3h;	A 65% B n/a

...Expand

: 186581-53-3, 908094-01-9
diazomethane

: 556-89-8
nitrourea

: 598-57-2
methylnitroamine

: 186581-53-3, 908094-01-9
diazomethane

: N-nitro-N'-ethyl-urea

A: 598-57-2
methylnitroamine

B: 4164-28-7
N-nitrodimethylamine

C: 109-90-0
ethyl isocyanate

...Expand

: 687-48-9
ethyl N,N-dimethylcarbamate

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With nitric acid nimmt das erhaltene Nitromethylurethan mit Aether auf und leitet in die aether. Loesung trocknes NH3 ein;

: 14442-54-7
methyl-nitro-carbamic acid methyl ester

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With diethyl ether; ammonia der Entstandene Niederschlag des Ammoniumsalzes mit Aether gewaschen und durch Kochen mit Alkohol zersetzt wird;

: 91086-49-6
bis-(N-methyl-N-ethoxycarbonylamino)methane

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With nitric acid at -8℃; Leiten von NH3 in die aether.Loesung des Reaktionsprodukts;

: 14760-99-7
N,N’-dimethyl-N,N’-dinitrooxalamide

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With ammonium hydroxide Entsteht als Ammoniumsalz;
With barium dihydroxide; water man faellt freien Baryt durch CO2, dammpft die Loesung ein, versetzt den Rueckstand mit der theoretischen Menge Schwefelsaeure und nimmt das freie Methylnitramin in Aether auf;
With ammonia at 5 - 20℃; under 6000.6 Torr; for 0.333333h; Autoclave;	0.61 g

: 60-29-7
diethyl ether

: N-methyl-N-nitro-N'-phenyl-urea

: 62-53-3
aniline

A: 598-57-2
methylnitroamine

B: 603-54-3
N,N-diphenylurea

...Expand

: 598-50-5
N-Methylurea

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
Nitrierung von Methylharnstoff und letzterer zerfaellt bei der Aufarbeitung des Reaktionsprodukts durch Behandeln mit Ammoniak;

: 74-89-5
methylamine

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
(i) nBuLi, Et2O, (ii) EtONO2; Multistep reaction;

: 110-89-4
piperidine

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

A: 598-57-2
methylnitroamine

B: 3506-37-4
(E)-1-phenyl-3-(piperidin-1-yl)prop-2-en-1-one

Conditions

Conditions	Yield
In ethanol at 35 - 40℃; for 3h; Yield given;

...Expand

: 14442-60-5
N-methyl-N-nitroacetamide

A: 598-57-2
methylnitroamine

B: 64-19-7
acetic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism; Kinetics; ΔS(excit.);
With phosphate buffer In water at 25℃; Rate constant; Kinetics; Mechanism; effect of various catalysts in various aqueous buffers, dependence of the rate constant on the pH;

: 41404-94-8
N-methyl-N-vinylnitroamine

A: 598-57-2
methylnitroamine

B: 75-07-0
acetaldehyde

Conditions

Conditions	Yield
With hydrogenchloride In chloroform at 20℃;	A 0.03 g B n/a

: 59476-39-0
N-methyl-N-nitrobenzamide

A: 598-57-2
methylnitroamine

B: 65-85-0
benzoic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism; Kinetics; ΔS(excit.);
With phosphate buffer In water at 25℃; Kinetics; Thermodynamic data; Mechanism; effect of various catalysts in various aqueous buffers, dependence of the rate constant on the pH, effect of aromatic substituents;

: 90110-19-3
4-Chlor-N-nitro-benzoesaeure-methylamid

A: 598-57-2
methylnitroamine

B: 74-11-3
para-chlorobenzoic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism;

: 97661-71-7
N-methyl-4-methyl-N-nitrobenzamide

A: 598-57-2
methylnitroamine

B: 99-94-5
p-Toluic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism;

: 97661-72-8
C9H10N2O4

A: 598-57-2
methylnitroamine

B: 100-09-4
4-methoxybenzoic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism; Kinetics; ΔS(excit.);
With phosphate buffer In water at 25℃; Kinetics; Thermodynamic data;

: N-methyl-N-nitrobenzamide

A: 598-57-2
methylnitroamine

B: 21048-30-6
benzoic acid-O18

C: 65-85-0
benzoic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Product distribution; Mechanism;

...Expand

: 127843-54-3
C9H7F3N2O3

A: 598-57-2
methylnitroamine

B: 455-24-3
4-trifluoromethylbenzoic acid

Conditions

Conditions	Yield
With water; sulfuric acid at 25℃; Rate constant; Mechanism;

: 92667-06-6
1-<(Methyl)(nitro)amino>ethylacetat

A: 598-57-2
methylnitroamine

B: 75-07-0
acetaldehyde

C: 64-19-7
acetic acid

Conditions

Conditions	Yield
With water-d2 for 2h; Product distribution; complete hydrolysis; investigation of half life time;

...Expand

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

A: 598-57-2
methylnitroamine

B: 2458-26-6
3-phenylpyrazole

Conditions

Conditions	Yield
With hydrazine hydrate In ethanol at 35 - 40℃; for 3h; Yield given;

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

: 109-89-7
diethylamine

A: 598-57-2
methylnitroamine

B: 23674-58-0
(E)-3-(diethylamino)-1-phenylprop-2-en-1-one

Conditions

Conditions	Yield
In ethanol at 35 - 40℃; for 3h; Yield given;

...Expand

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

: 62-53-3
aniline

A: 598-57-2
methylnitroamine

B: 37418-64-7
(E)-1-phenyl-3-(phenylamino)prop-2-en-1-one

Conditions

Conditions	Yield
In ethanol at 35 - 40℃; for 3h; Yield given;

...Expand

: 74-88-4
methyl iodide

nitro urethane silver: nitro urethane silver

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With diethyl ether Behandeln die N-Nitro-N-methyl-urethan wie bei vorstehender Bildungsweise mit Ammoniakgas;

N-nitro-N-methyl-p-toluenesulfonamide: N-nitro-N-methyl-p-toluenesulfonamide

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With sodium hydroxide

N-nitro-N-methyl-urea: N-nitro-N-methyl-urea

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With potassium hydroxide
With barium dihydroxide
With ammonia

sodium methyl isodiazotate: sodium methyl isodiazotate

: 598-57-2
methylnitroamine

Conditions

Conditions	Yield
With alkalies; potassium hexacyanoferrate(III)

: 856205-95-3
N,N'-dimethyl-N,N'-dinitro-methanedisulfonamide

: 7664-41-7
ammonia

A: 598-57-2
methylnitroamine

B: 183996-57-8
methylene disulfonamide

...Expand

: 856205-95-3
N,N'-dimethyl-N,N'-dinitro-methanedisulfonamide

alkaline solution: alkaline solution

A: 598-57-2
methylnitroamine

B: 503-40-2
methanedisulfonic acid

...Expand

: 598-57-2
methylnitroamine

: 2,2-bis(2-methoxy-1-oxidodiazenyl)ethyl trifluoroacetate

: 102526-33-0
1,1-bis(N-oxide-N'-methoxydiazenyl)-3-nitro-3-azabutane

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid In ethyl acetate at 20℃; for 24h;	94%

: 598-57-2
methylnitroamine

: 124-63-0
methanesulfonyl chloride

: 34170-43-9
N-nitro-N-methylmethanesulfonamide

Conditions

Conditions	Yield
With triethylamine In acetonitrile at 20℃; for 4h;	92%

: 598-57-2
methylnitroamine

: 2850-26-2
(toluene-4-sulfonylmethyl)-carbamic acid ethyl ester

: 103635-49-0
C5H11N3O4

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 2h; Ambient temperature;	90%

: 598-57-2
methylnitroamine

: 3696-52-4
Ethyl-N-<α-(p-toluolsulfonyl)-benzyl>-carbamat

: 103635-53-6
α-Ethoxycarbonylaminobenzyl-methylnitramin

Conditions

Conditions	Yield
With triethylamine In dichloromethane 1.) 30 min, reflux, 2.) 3 h, room temp.;	89%

: 598-57-2
methylnitroamine

: 14674-22-7
N-(p-Toluolsulfonylmethyl)-benzamid

: 103635-47-8
C9H11N3O3

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 2h; Ambient temperature;	89%

: 598-57-2
methylnitroamine

: 14674-23-8
N-<α-(p-Toluolsulfonyl)-benzyl>-benzamid

: 103635-51-4
C15H15N3O3

Conditions

Conditions	Yield
With triethylamine In dichloromethane 1.) 30 min, reflux, 2.) 3 h, room temp.;	88%

: 50-00-0
formaldehyd

: 598-57-2
methylnitroamine

: 13232-00-3
2,4-dinitro-2,4-diazapentane

Conditions

Conditions	Yield
With sulfuric acid at 0 - 5℃; for 0.5h;	85%
With sulfuric acid at 18℃; Product distribution; time and the ratio of the reagents dependence;
With sulfuric acid
With hydrogen cation

: 598-57-2
methylnitroamine

: 38792-42-6
N-(chloromethyl)benzamide

: 103635-47-8
C9H11N3O3

Conditions

Conditions	Yield
With triethylamine In acetone for 2h; Ambient temperature;	85%

: 598-57-2
methylnitroamine

: C7H9O(1-)*C5H5(1-)*Fe(2+)

: C8H11N2O2(1-)*C5H5(1-)*Fe(2+)

Conditions

Conditions	Yield
In acetic acid at 60℃; for 2h; Product distribution;	83%

: 598-57-2
methylnitroamine

: 3623-15-2
phenyl propargyl ketone

: 99647-88-8
1-phenyl-3-(methylnitroamino)-2-propen-1-one

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 50℃; for 2.5h;	79%

: 598-57-2
methylnitroamine

: 82670-28-8
N-(chloromethyl)-N-methylmethanesulfonamide

: 80552-93-8
C4H11N3O4S

Conditions

Conditions	Yield
With triethylamine In diethyl ether at 20℃; for 3h;	76%

: 598-57-2
methylnitroamine

: 129-66-8
2,4,6-trinitrobenzoic acid

: 15012-38-1
methyl 2,4,6-trinitrobenzoate

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane at 20℃; for 1h;	75%

: 50-00-0
formaldehyd

: 598-57-2
methylnitroamine

potassium, sodium or ammonium N-(3-hydroxypropyl)sulfamate: potassium, sodium or ammonium N-(3-hydroxypropyl)sulfamate

: 4,6-dinitro-4,6-diazaheptyl nitrate

Conditions

Conditions	Yield
Stage #1: formaldehyd; methylnitroamine; potassium, sodium or ammonium N-(3-hydroxypropyl)sulfamate In ethanol; water pH=5.5; Stage #2: With nitric acid at -20℃; for 1h;	75%

...Expand

: 598-57-2
methylnitroamine

: 3433-80-5
1-Bromo-2-bromomethyl-benzene

A: C8H9BrN2O2

B: 2-Brombenzyl-methylnitramin

Conditions

Conditions	Yield
With sodium 1.) EtOH, 2.) reflux, 10 min; room temp., 10 h;	A n/a B 73%

...Expand

: 598-57-2
methylnitroamine

: 102526-24-9, 128957-61-9
2-acetoxyethylidenedi(N'-methoxydiazene) di-N-oxide

: 102526-33-0
1,1-bis(N-oxide-N'-methoxydiazenyl)-3-nitro-3-azabutane

Conditions

Conditions	Yield
With triethylamine In ethanol at 70 - 78℃; for 1.5h; Heating;	72%

: 598-57-2
methylnitroamine

: 102526-26-1
C4H9N5O7

: 102526-33-0
1,1-bis(N-oxide-N'-methoxydiazenyl)-3-nitro-3-azabutane

Conditions

Conditions	Yield
With triethylamine In ethanol at 70 - 78℃; for 1.5h; Heating;	72%

: 50-00-0
formaldehyd

: 598-57-2
methylnitroamine

potassium, sodium or ammonium N-(2-hydroxyethyl)sulfamate: potassium, sodium or ammonium N-(2-hydroxyethyl)sulfamate

: 201596-34-1
3,5-dinitro-3,5-diazahexyl nitrate

Conditions

Conditions	Yield
Stage #1: formaldehyd; methylnitroamine; potassium, sodium or ammonium N-(2-hydroxyethyl)sulfamate In ethanol; water pH=5.5; Stage #2: With nitric acid at -20℃; for 1h;	68%

...Expand

: 598-57-2
methylnitroamine

: 515114-33-7
5-iodomethyl-3-nitrooxazolidine

: 5-(methyl-N-nitroaminomethyl)-3-nitrooxazolidine

Conditions

Conditions	Yield
With sodium carbonate In N,N-dimethyl-formamide at 85 - 90℃; for 8h;	67%

: 598-57-2
methylnitroamine

: 80369-00-2
N-isopropyl-N-chloromethylmethanesulfamide

: 80552-94-9
C6H15N3O4S

Conditions

Conditions	Yield
With triethylamine In diethyl ether at 20℃; for 3h;	61%

: 598-57-2
methylnitroamine

: 7338-94-5
1,3-diphenyl-2-propynone

: 90104-60-2
1,3-diphenyl-3-(methylnitroamino)-2-propen-1-one

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 50℃; for 2.5h;	58%

: 50-00-0
formaldehyd

: 598-57-2
methylnitroamine

potassium, sodium or ammonium N-(2-hydroxypropyl)sulfamate: potassium, sodium or ammonium N-(2-hydroxypropyl)sulfamate

: 1-methyl-3,5-dinitro-3,5-diazahexyl nitrate

Conditions

Conditions	Yield
Stage #1: formaldehyd; methylnitroamine; potassium, sodium or ammonium N-(2-hydroxypropyl)sulfamate In ethanol; water pH=5.5; Stage #2: With nitric acid at -20℃; for 1h;	55%

...Expand

: 111-34-2
-butyl vinyl ether

: 598-57-2
methylnitroamine

: n-butyl 3-nitro-3-azabut-2-yl ether

Conditions

Conditions	Yield
With sulfuric acid In dichloromethane at 30 - 35℃; for 6h; Addition;	52.3%

: 598-57-2
methylnitroamine

: 15814-30-9
1,5-diphenyl-penta-1,4-diyn-3-one

: 90104-51-1
1,5-diphenyl-1,5-di(methylnitroamino)-1,4-pentadien-3-one

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 50℃; for 1h;	52%

: 598-57-2
methylnitroamine

: 90104-50-0
1,5-diphenyl-1-(methylnitroamino)-1-penten-4-yn-3-one

: 90104-51-1
1,5-diphenyl-1,5-di(methylnitroamino)-1,4-pentadien-3-one

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 50℃; for 1h;	52%

: 598-57-2
methylnitroamine

: 4761-00-6
2,4,6-trimethylbenzylbromide

A: C8H9BrN2O2

B: 2,4,6-Trimethylbenzyl-methylnitramin

Conditions

Conditions	Yield
With sodium 1.) EtOH, 2.) reflux; room temp.;	A n/a B 50%

...Expand

: 598-57-2
methylnitroamine

: 1794-48-5
1-bromo-3-phenylprop-2-yne

: 90104-53-3
1-phenyl-3-(methylnitroamino)-1-propyne

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 60 - 70℃; for 3h;	50%

: 50-00-0
formaldehyd

: 598-57-2
methylnitroamine

: 18139-02-1
2-fluoro-2,2-dinitro-ethylamine

: 123202-13-1
1-fluoro-1,1,5-trinitro-3,5-diazahexane

Conditions

Conditions	Yield
In methanol at 50 - 60℃; for 2h;	49%

...Expand

: 598-57-2
methylnitroamine

: 15814-30-9
1,5-diphenyl-penta-1,4-diyn-3-one

: 90104-50-0
1,5-diphenyl-1-(methylnitroamino)-1-penten-4-yn-3-one

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 50℃; for 2.5h;	48%

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5986-55-0

1,6-Methanonaphthalen-1(2H)-ol,octahydro-4,8a,9,9-tetramethyl-, (1R,4S,4aS,6R,8aS)-

59865-82-6

Ethanethioamide,2-(phenylthio)-

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