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Merck
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文件

226157

Sigma-Aldrich

N-羟基氨基甲酸叔丁酯

≥98%

别名:

N-叔丁氧羰基羟胺

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About This Item

线性分子式:
(CH3)3COCONHOH
CAS号:
36016-38-3
分子量:
133.15
Beilstein:
1756546
EC號碼:
252-836-2
MDL號碼:
MFCD00002107
分類程式碼代碼:
12352100
PubChem物質ID:
24853547
NACRES:
NA.22

化驗

≥98%

形狀

solid

mp

53-55 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

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 密鑰

DRDVJQOGFWAVLH-UHFFFAOYSA-N

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相关类别

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

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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)
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
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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