226157
N-Boc-hydroxylamine
≥98%
Synonym(s):
tert-Butyl N-hydroxycarbamate
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About This Item
Linear Formula:
(CH3)3COCONHOH
CAS Number:
Molecular Weight:
133.15
Beilstein:
1756546
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥98%
form
solid
mp
53-55 °C (lit.)
storage temp.
2-8°C
SMILES string
CC(C)(C)OC(=O)NO
InChI
1S/C5H11NO3/c1-5(2,3)9-4(7)6-8/h8H,1-3H3,(H,6,7)
InChI key
DRDVJQOGFWAVLH-UHFFFAOYSA-N
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Related Categories
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthetic Communications, 22, 2579-2579 (1992)
Brian S Bodnar et al.
The Journal of organic chemistry, 72(10), 3929-3932 (2007-04-14)
The addition of azides to acylnitroso hetero-Diels-Alder cycloadducts derived from cyclopentadiene affords exo-triazolines in excellent yield. The reaction is greatly affected by the level of alkene strain, while sterically demanding azides do not hinder the reaction. Conversion of the triazolines
Tetrahedron Letters, 33, 5055-5055 (1992)
Useful hydroxylamine derivatives for the synthesis of hydroxamic acids.
Tetrahedron Letters, 33(35), 5055-5058 (1992)
Timothy A Wencewicz et al.
Journal of medicinal chemistry, 54(19), 6843-6858 (2011-08-24)
The discovery, syntheses, and structure-activity relationships (SAR) of a new family of heterocyclic antibacterial compounds based on N-alkyl-N-(pyridin-2-yl)hydroxylamine scaffolds are described. A structurally diverse library of ∼100 heterocyclic molecules generated from Lewis acid-mediated nucleophilic ring-opening reactions with nitroso Diels-Alder cycloadducts
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