ChemicalBook Product Catalog Chemical Reagents Organic reagents Hydroxylamine N,O-Dimethylhydroxylamine hydrochloride

N,O-Dimethylhydroxylamine hydrochloride

N,O-Dimethylhydroxylamine hydrochloride Basic information
Product Name:N,O-Dimethylhydroxylamine hydrochloride
Synonyms:N,O-DiMethylhydroxylaMine Hyd;MethanaMine,N-Methoxy-, hydrochloride (1:1);N,O-Dimethylhydroxylamine Hydrochloride;N,O-dimehtylhydroxylamine.HCL;N,O-Dimethylhydroxylamine hydrochloride≥ 99% (GC);O-Dimethylhydroxylamine hydrochloride;CAS:6638-79-5;n,o-dimethylhydroxylamine hydrochloride cas 6638-79-5
CAS:6638-79-5
MF:C2H8ClNO
MW:97.54
EINECS:229-642-1
Product Categories:Aliphatics;Amines;Amination;Active Esters/Additives;Coupling;Synthetic Reagents;API intermediates;Hydroxylamines;Hydroxylamines (N-Substituted);Hydroxylamines (O-Substituted);Synthetic Organic Chemistry;1;3;bc0001;6638-79-5
Mol File:6638-79-5.mol
N,O-Dimethylhydroxylamine hydrochloride Structure
N,O-Dimethylhydroxylamine hydrochloride Chemical Properties
Melting point 112-115 °C
storage temp. Store below +30°C.
solubility DMSO, Methanol
form Crystalline Powder or Crystals
color White to off-white
Water Solubility SOLUBLE
Sensitive Hygroscopic
BRN 3650353
InChIInChI=1S/C2H7NO.ClH/c1-3-4-2;/h3H,1-2H3;1H
InChIKeyUSZLCYNVCCDPLQ-UHFFFAOYSA-N
SMILESN(C)OC.Cl
CAS DataBase Reference6638-79-5(CAS DataBase Reference)
EPA Substance Registry SystemMethanamine, N-methoxy-, hydrochloride (6638-79-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/38-36/37/38
Safety Statements 26-36-24/25
WGK Germany 3
TSCA Yes
HS Code 29280090
MSDS Information
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N,O-Dimethylhydroxylamine hydrochloride English
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N,O-Dimethylhydroxylamine hydrochloride Usage And Synthesis
Chemical PropertiesN,O-Dimethylhydroxylamine hydrochloride is white to off-white crystals or crystalline powder
UsesN,O-Dimethylhydroxylamine hydrochloride is used for preparation of an inhibitor of the NLS-derived BC peptides.
UsesN,O-Dimethylhydroxylamine hydrochloride is used as a reagent in the preparation of 2-acyloxazoles from 2-oxazolemagnesium chloride and N-methoxy-N-methyl-3-oxo-butyramide from diketene. It is also used in amide coupling reactions to form Weinreb amides, which are useful in the Weinreb ketone synthesis. In addition, it is used in the preparation of an inhibitor of the NLS-derived BC peptides.
UsesReagent for the preparation of Weinreb amides recently used in the synthesis of 2-acyloxazoles from 2-oxazolemagnesium chloride.
N,O-Dimethylhydroxylamine hydrochloride Preparation Products And Raw materials
Preparation Products1-(4-ACETYLPIPERIDINO)ETHAN-1-ONE-->N-methylquinolin-2-amine-->DIETHYL (N-METHOXY-N-METHYLCARBAMOYLMETHYL)PHOSPHONATE-->N-Methoxy-N-methylnicotinamide-->N-Methoxy-N,1-diMethylpiperidine-4-carboxaMide-->N,N-DIMETHYLHEXANAMIDE-->4,N-DIMETHYL-N-METHOXYBENZAMIDE-->N-methoxy-N-methyl-2-(4-nitrophenyl)acetamide-->(R)-1-Boc-2-[Methoxy(Methyl)carbaMoyl]pyrrolidine-->4-IODO-N-METHOXY-N-METHYL-BENZAMIDE -->TERT-BUTYL 3-(METHOXY(METHYL)CARBAMOYL)PYRROLIDINE-1-CARBOXYLATE-->5-Isoxazolecarboxamide,N-methoxy-N-methyl-(9CI)
2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL N-(4-CHLOROPHENYL)CARBAMATE METHAZOLE N-(2,2,2-TRICHLOROETHOXYCARBONYLOXY)SUCCINIMIDE N-([(4-CHLOROANILINO)CARBONYL]OXY)-2-(4,5-DICHLORO-1H-IMIDAZOL-1-YL)ACETAMIDE N,O-Dimethylhydroxylamine hydrochloride Linuron Clomazone VINYL ACETOXY TRIMETHYL AMMONIUM CHLORIDE N,N-BIS(2-CHLORO-6-FLUOROBENZYL)-N-(([(1,2,2-TRICHLOROVINYL)AMINO]CARBONYL)OXY)AMINE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL N-PHENYLCARBAMATE CHLORBROMURON N-[(2-CHLOROACETYL)OXY]-N,N-BIS(4-CHLOROBENZYL)AMINE N-[(4-CHLOROBENZOYL)OXY]-2-(4,5-DICHLORO-1H-IMIDAZOL-1-YL)ACETAMIDE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL N-ISOPROPYLCARBAMATE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 2-CHLOROBENZOATE N-(2-Chlorobenzyloxycarbonyloxy)succinimide 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 4-CHLOROBENZOATE MONOLINURON
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