412791
N,O-Di-Boc-hydroxylamine
97%
Synonym(s):
N,O-Bis(tert-butoxycarbonyl)hydroxylamine, tert-Butyl N-(tert-butoxycarbonyloxy)carbamate
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About This Item
Linear Formula:
(CH3)3COCONHOCOOC(CH3)3
CAS Number:
Molecular Weight:
233.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
285-055-0
Beilstein/REAXYS Number:
1794022
MDL number:
Assay:
97%
InChI key
AGOSGCWATIJZHQ-UHFFFAOYSA-N
InChI
1S/C10H19NO5/c1-9(2,3)14-7(12)11-16-8(13)15-10(4,5)6/h1-6H3,(H,11,12)
SMILES string
CC(C)(C)OC(=O)NOC(=O)OC(C)(C)C
assay
97%
Quality Level
functional group
amine
storage temp.
−20°C
Related Categories
Application
N,O-Di-Boc-hydroxylamine (N,O-Bis(tert-butoxycarbonyl)hydroxylamine) may be used for the synthesis of the following:
- 5-lipoxygenase inhibitor LY280810
- hydroxylamines
- hydroxamic acids,
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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The use of N, O-bis (tert-butoxycarbonyl)-hydroxylamine in the synthesis of N-hydroxylamines and hydroxamic acids.
Staszak MA and Doecke CW.
Tetrahedron Letters, 35(23), 6021-6024 (1994)
A facile synthesis of N, O-bis (tert-butoxycarbonyl)-hydroxylamine.
Staszak MA and Doecke CW.
Tetrahedron Letters, 34(44), 7043-7044 (1993)
A convenient method for the preparation of hydroxamic acids.
Reddy AS, et al.
Tetrahedron Letters, 41(33), 6285-6288 (2000)
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