O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Basic information
- Product Name:
- O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
- Synonyms:
-
- O-(tert-Butyl)hydroxylamine hydrochloride 98%
- O-T-BUTYLHYDROXYLAMINE HYDROCHLORIDE
- O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
- O-Tert-ButylhydroxylamineHCl
- 2-Aminooxy-2-methylpropane hydrochloride
- O-(1,1-Dimethylethyl)hydroxylamine hydrochloride
- tert-Butoxyamine hydrochloride
- HydroxylaMine,O-(1,1-diMethylethyl)-, hydrochloride (1:1)
- CAS:
- 39684-28-1
- MF:
- C4H12ClNO
- MW:
- 125.6
- EINECS:
- 254-590-1
- Product Categories:
-
- Building Blocks
- Chemical Synthesis
- Hydroxylamines
- Nitrogen Compounds
- Nitrogen Compounds
- Organic Building Blocks
- Organic Building Blocks
- Mol File:
- 39684-28-1.mol
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Chemical Properties
- Melting point:
- 158-159 °C(lit.)
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- H2O: soluble0.5g/10 mL
- form
- powder to crystal
- color
- White to Almost white
- BRN
- 3668106
MSDS
- Language:English Provider:SigmaAldrich
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Usage And Synthesis
Chemical Properties
White crystalline powder
Uses
Reactant involved in synthesis of biologically active molecules including:• ;CGS 25966 derivatives for use as MMP inhibitors1• ;Imidazolidinedione derivatives for use as antimalarial treatments2• ;Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3• ;Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:• ;Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5• ;Double allylic alkylation of indole-2-hydroxamates6• ;SN2 substitution reactions at amide nitrogens7• ;Photoc
Uses
O-tert-Butylhydroxylamine Hydrochloride is an reactant used in various synthesis of biologically active molecules such as camptothecin derivatives that exerts anti-tumor activity, oxime derivatives as GPR119 agonists and their preparation and highly Potent Matrix Metalloproteinase Inhibitors.
Uses
Reactant involved in synthesis of biologically active molecules including:
- CGS 25966 derivatives for use as MMP inhibitors
- Imidazolidinedione derivatives for use as antimalarial treatments
- Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists
- Rab proteins for isoprenylation and geranylgeranylation inhibition
Reactant involved in:
- Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents
- Double allylic alkylation of indole-2-hydroxamates
- SN2 substitution reactions at amide nitrogens
- Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDESupplier
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O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE(39684-28-1)Related Product Information
- Dimethylamine hydrochloride
- HYDROXYLAMINE
- O-Benzoyl-N-tert-butylhydroxylamine Hydrochloride
- O-Acetyl-N-tert-butylhydroxylamine Hydrochloride
- Cefmepidium chloride
- 3-(2-CHLORO-PHENYL)-5-METHYL-4,5-DIHYDRO-ISOXAZOLE-5-CARBOXYLIC ACID
- O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
- 1-Carboxy-1-methylethoxyammonium chloride
- 1-[[(6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)[(1-carboxy-1-methylethoxy)imino]acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]pyridinium chloride monohydrochloride