O-tert-Butylhydroxylamine hydrochloride

• Catalog No.: B5765
• CAS Number: 39684-28-1
• M. F.: C4H12ClNO
• M. W.: 125.59718
• Purity: ≥99%

SYNONYMS

• Title: O-叔丁基羟胺 盐酸盐
• IUPAC name: O-tert-butylhydroxylamine hydrochloride
• IUPAC Traditional name: O-tert-butylhydroxylamine hydrochloride
• Synonyms: tert-Butoxyamine hydrochloride; O-(1,1-Dimethylethyl)hydroxylamine hydrochloride; 2-Aminooxy-2-methylpropane hydrochloride

DATABASE IDS

• Beilstein Number: 3668106
• MDL Number: MFCD00043272
• PubChem SID: 24891858
• CAS Number: 39684-28-1
• EC Number: 254-590-1

PROPERTIES

• Linear Formula: (CH3)3CONH2 · HCl
• Purity: ≥99%
• GHS Signal Word: Warning
• GHS Hazard statements: H228
• European Hazard Symbols: Flammable (F)
• Personal Protective Equipment: Eyeshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
• GHS Precautionary statements: P210
• RID/ADR: UN 1325 4.1/PG 3
• Risk Statements: 11
• Hazard Class: 4.1
• UN Number: 1325
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in glass bottle
Application
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
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8

Description (简体中文)

包装
5 g in glass bottle
Application
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
• Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines8