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226157

Sigma-Aldrich

N-Boc-hydroxylamine

≥98%

Synonym(s):

tert-Butyl N-hydroxycarbamate

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About This Item

Linear Formula:
(CH3)3COCONHOH
CAS Number:
36016-38-3
Molecular Weight:
133.15
Beilstein/REAXYS Number:
1756546
EC Number:
252-836-2
MDL number:
MFCD00002107
UNSPSC Code:
12352100
PubChem Substance ID:
24853547
NACRES:
NA.22

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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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Useful hydroxylamine derivatives for the synthesis of hydroxamic acids.
Tetrahedron Letters, 33(35), 5055-5058 (1992)
Tetrahedron Letters, 33, 5055-5055 (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
Synthetic Communications, 22, 2579-2579 (1992)
M J Lee et al.
Journal of medicinal chemistry, 35(20), 3648-3652 (1992-10-02)
In the preceding paper, analogs of chlorpropamide with an OMe substituent on the sulfonamide nitrogen were shown to inhibit aldehyde dehydrogenase (AlDH), and it was postulated that these compounds were bioactivated by O-demethylation to release nitroxyl (HN = O, nitrosyl
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