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Cas:1117-97-1
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inquiryN-methoxymethylamine Basic information Product Name: N-methoxymethylamine Synonyms: N-methoxymethylamine;Methylmethoxyamine;N-Methoxymethanamine;O,N-Dimethylhydroxy
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Cas:1117-97-1
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Cas:1117-97-1
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Cas:1117-97-1
Min.Order:1 Gram
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Appearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By
Cas:1117-97-1
Min.Order:100 Gram
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The process is mature and can be mass produced to 100 kg, with good quality and purity up to 99%.The product has a large stock and can be supplied stably. Package:bottle Application:Drug R&D Transportation:Sealed drying(25℃) Port:ShangHai
Cas:1117-97-1
Min.Order:1 Gram
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inquiryISO/factory/goodqualityAppearance:off white Storage:Dry,cool place Package:drum Application:active pharmaceutical ingredients Transportation:by air/sea/express Port:shenzhen/shanghai
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Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
Cas:1117-97-1
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou
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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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Cas:1117-97-1
Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiryBest quality & Attractive price & Professional service; Trial & Pilot & CommercialHenan Fine Chemicals Co., LTD. is a diversified technology - oriented integrated company, which mainly concentrates on fine chemicals. Our company is committed to becom
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
please contact us to confirm the required quantity and quote, we will provide you with COA,NMR,HPLC and other relevant informationAppearance:Yellow crystals Storage:Store in a cool place. Keep container tightly closed in a dry and well-ventilated pla
Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide distillation; | 92% |
With triethanolamine at 150℃; | 81% |
With triethanolamine In ethylene glycol at 150℃; | 81% |
Conditions | Yield |
---|---|
With hydrogenchloride |
Conditions | Yield |
---|---|
With aniline at 150℃; |
N,O-Dimethylhydroxymethan
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
at 298℃; Thermodynamic data; rearrangement of N-oxide to O-alkyl hydroxylamines , ΔH, ΔS, ΔG; |
N-nitroso-N,O-dimethylhydroxylamine
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With perchloric acid; ammonium sulfamate; sodium thiocyanide at 50℃; Rate constant; | |
With 2,2-dicloroethanol In cyclohexane at 25℃; Kinetics; Equilibrium constant; Decomposition; |
β-(N-methyl-N-methoxyamine)-α-nitrostilbene
A
(E)-β-Methoxy-α-nitrostilbene
B
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
In water; dimethyl sulfoxide at 20℃; Equilibrium constant; |
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With potassium hydroxide durch Verseifung; |
Conditions | Yield |
---|---|
Verseifung; |
N-Methoxy-N-methylacetamide
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
In ethanol | |
With sulfuric acid at 76℃; for 5h; |
methyl methoxy methyl carbamate
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water |
dimethyl sulfate
A
O-Methylhydroxylamin
B
N,N-dimethylhydroxylamine
C
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With hydroxylamine hemisulfate; sodium carbonate; sodium hydroxide In water at 2 - 5℃; for 2h; |
methylene chloride
A
O-Methylhydroxylamin
B
N,N-dimethylhydroxylamine
C
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With hydroxylamine hydrochloride; sodium carbonate; sodium hydroxide In water at 2 - 5℃; for 2h; Concentration; Temperature; |
S-2-azido-3-(N-Boc-piperidyl)-propionic acid
N,0-dimethylhydroxylamine
4-[2-azido-2-(methoxy-methyl-carbamoyl)-ethyl]-piperidine-1-carboxylic acid tert-butyl ester
Conditions | Yield |
---|---|
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In dichloromethane | 100% |
N-(tert-butyloxycarbonyl)-L-isoleucine
N,0-dimethylhydroxylamine
N-(tert-butoxycarbonyl)-L-isoleucine N'-methoxy-N'-methylamide
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at -15℃; for 1h; | 100% |
Stage #1: N-(tert-butyloxycarbonyl)-L-isoleucine; N,0-dimethylhydroxylamine With triethylamine at 0℃; Stage #2: With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine | 95% |
With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine In dichloromethane | 94% |
N-(tert-butoxycarbonyl)-D-proline
N,0-dimethylhydroxylamine
[tert-butyl (R)-2-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate]
Conditions | Yield |
---|---|
Stage #1: N-(tert-butoxycarbonyl)-D-proline With HATU In dichloromethane at 0℃; for 1h; Stage #2: N,0-dimethylhydroxylamine With N-ethyl-N,N-diisopropylamine In dichloromethane at 20 - 27℃; for 16h; | 100% |
Stage #1: N-(tert-butoxycarbonyl)-D-proline With 1,1'-carbonyldiimidazole In dichloromethane for 0.5h; Stage #2: N,0-dimethylhydroxylamine In dichloromethane | 52% |
Stage #1: N-(tert-butoxycarbonyl)-D-proline With 1,1'-carbonyldiimidazole In dichloromethane at 20℃; for 0.5h; Stage #2: N,0-dimethylhydroxylamine In dichloromethane at 20℃; | 52% |
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine |
2-methyl-3-phenylpropanoyl chloride
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
In tetrahydrofuran at -78℃; | 100% |
N,0-dimethylhydroxylamine
2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid
tert-butyl 6-(Methoxy(methyl)carbamoyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
Conditions | Yield |
---|---|
With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride In methanol at 20℃; | 100% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
(R)-4-(tert-butyloxycarbonyl)morpholine-2-carboxylic acid
N,0-dimethylhydroxylamine
tert-butyl (2R)-2-[methoxy(methyl)carbamoyl]morpholine-4-carboxylate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide | 100% |
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine In dichloromethane | 85% |
4-methoxy-3-cyanobenzoic acid
N,0-dimethylhydroxylamine
3-cyano-N,4-dimethoxy-N-methylbenzamide
Conditions | Yield |
---|---|
With triethylamine; HATU In dichloromethane at 20℃; for 2h; Inert atmosphere; | 100% |
pent-4-enoyl chloride
N,0-dimethylhydroxylamine
N-methoxy-N-methyl-4-pentenamide
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; for 1.5h; Inert atmosphere; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; | 3.54 g |
4-bromo-2-picolinic acid
N,0-dimethylhydroxylamine
4-bromo-pyridine-2-carboxylic acid N-methoxy-N-methyl-amide
Conditions | Yield |
---|---|
With triethylamine; HATU In N,N-dimethyl-formamide at 20℃; for 2h; | 100% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
1-benzyloxycarbonylpiperidine-4-carboxylic acid
N,0-dimethylhydroxylamine
4-(N-methoxy-N-methyl-carbamoyl)-piperidine-1-carboxylic acid benzyl ester
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 20℃; for 15h; | 100% |
1-(tert-butoxycarbonyl)-4-methylpiperidine-3-carboxylic acid
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With triethylamine; HATU In dichloromethane for 14h; Cooling with ice; | 100% |
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane for 14h; Reagent/catalyst; Solvent; | 100% |
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane for 14h; | 100% |
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane for 14h; Solvent; Reagent/catalyst; | 100% |
Conditions | Yield |
---|---|
With triethylamine; 1,1'-carbonyldiimidazole In tetrahydrofuran; acetonitrile at 20 - 80℃; for 168h; Inert atmosphere; | 100% |
2-nitro-4-dichloromethylsulfonylchlorobenzene
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With triethylamine In benzene Heating; | 99.2% |
N-tert-butoxycarbonyl-L-phenylalanine
N,0-dimethylhydroxylamine
Boc-Phe-OH N,O-dimethyl hydroxamate
Conditions | Yield |
---|---|
With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In dichloromethane | 99% |
With 1,1'-carbonyldiimidazole | 98% |
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate | 95% |
N,0-dimethylhydroxylamine
para-chlorobenzoic acid
4-chloro-N-methoxy-N-methylbenzamide
Conditions | Yield |
---|---|
Stage #1: N,0-dimethylhydroxylamine; para-chlorobenzoic acid In toluene at 0℃; for 0.166667h; Stage #2: With phosphorus trichloride In toluene at 20 - 60℃; for 0.5h; | 99% |
With 1,1'-carbonyldiimidazole | |
With triethylamine; 1,1'-carbonyldiimidazole |
phenylacetyl chloride
N,0-dimethylhydroxylamine
N-methoxy-N-methyl-2-phenylacetamide
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; for 1.16667h; Inert atmosphere; | 99% |
With pyridine In dichloromethane | 98% |
With diaminopyridine; triethylamine In dichloromethane at 20℃; | 78.7% |
65% | |
With pyridine In chloroform |
Conditions | Yield |
---|---|
In ethanol for 4h; Heating; | 99% |
tert-butyl N-(1S,5E)-1-methyl-6-[(1S,4R,5S)-3-oxo-2-oxabicyclo[2.2.1]hept-5-yl]-5-hexenylcarbamate
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With isopropylmagnesium chloride In tetrahydrofuran at -20℃; | 99% |
N6-Boc-N2-Cbz-lysine
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 19h; | 99% |
4-(4-methylphenoxy)benzoic acid
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
Stage #1: 4-(4-methylphenoxy)benzoic acid With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: N,0-dimethylhydroxylamine With triethylamine In N,N-dimethyl-formamide at 20℃; for 24h; | 99% |
Stage #1: 4-(4-methylphenoxy)benzoic acid With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: N,0-dimethylhydroxylamine In N,N-dimethyl-formamide at 20℃; for 24h; |
N,0-dimethylhydroxylamine
4-nitro-benzoic acid
N-methoxy-N-methyl-4-nitrobenzamide
Conditions | Yield |
---|---|
Stage #1: N,0-dimethylhydroxylamine; 4-nitro-benzoic acid In toluene at 0℃; for 0.166667h; Stage #2: With phosphorus trichloride In toluene at 20 - 60℃; for 0.5h; | 99% |
Conditions | Yield |
---|---|
Stage #1: 1-naphthalenecarboxylic acid; N,0-dimethylhydroxylamine In toluene at 0℃; for 0.166667h; Stage #2: With phosphorus trichloride In toluene at 20 - 60℃; for 0.5h; | 99% |
2-furanoic acid
N,0-dimethylhydroxylamine
N-methoxy-N-methyl-2-furancarboxamide
Conditions | Yield |
---|---|
Stage #1: 2-furanoic acid; N,0-dimethylhydroxylamine In toluene at 0℃; for 0.166667h; Stage #2: With phosphorus trichloride In toluene at 20 - 60℃; for 0.5h; | 99% |
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
In toluene at 90℃; Schlenk technique; Inert atmosphere; | 99% |
methyl cyclohexylcarboxylate
N,0-dimethylhydroxylamine
N-methoxy-N-methylcyclohexanecarboxamide
Conditions | Yield |
---|---|
With isopropylmagnesium chloride In tetrahydrofuran at -20 - 20℃; for 10h; Inert atmosphere; | 99% |
N,0-dimethylhydroxylamine
Conditions | Yield |
---|---|
With isopropylmagnesium chloride In tetrahydrofuran at -20℃; for 1h; | 99% |
With isopropylmagnesium chloride In tetrahydrofuran at -20℃; for 1h; Grignard Reaction; | 99% |
1-methyl-1H-benzo[d]imidazole-5-carboxylic acid
N,0-dimethylhydroxylamine
N-methoxy-N,1-dimethyl-1H-benzo[d]imidazole-5-carboxamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; HATU In dichloromethane at 0 - 20℃; | 98.78% |
phenylacetonitrile
N,0-dimethylhydroxylamine
N-methoxy-N-methyl-2-phenylacetamide
Conditions | Yield |
---|---|
Stage #1: phenylacetonitrile With potassium phosphate at 30℃; for 12h; pH=6; Enzymatic reaction; Stage #2: N,0-dimethylhydroxylamine at 20℃; for 0.5h; Concentration; Temperature; pH-value; | 98.5% |
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