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412791

Sigma-Aldrich

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:
85006-25-3
Molecular Weight:
233.26
Beilstein/REAXYS Number:
1794022
EC Number:
285-055-0
MDL number:
MFCD00034797
UNSPSC Code:
12352100
PubChem Substance ID:
24865823
NACRES:
NA.22

assay

97%

mp

67-70 °C (lit.)

storage temp.

−20°C

SMILES string

CC(C)(C)OC(=O)NOC(=O)OC(C)(C)C

InChI

1S/C10H19NO5/c1-9(2,3)14-7(12)11-16-8(13)15-10(4,5)6/h1-6H3,(H,11,12)

InChI key

AGOSGCWATIJZHQ-UHFFFAOYSA-N

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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,

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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A facile synthesis of N, O-bis (tert-butoxycarbonyl)-hydroxylamine.
Staszak MA and Doecke CW.
Tetrahedron Letters, 34(44), 7043-7044 (1993)
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 convenient method for the preparation of hydroxamic acids.
Reddy AS, et al.
Tetrahedron Letters, 41(33), 6285-6288 (2000)

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