所有图片(1)
About This Item
线性分子式:
(CH3)3COCONHOH
CAS号:
分子量:
133.15
Beilstein:
1756546
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
品質等級
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
正在寻找类似产品? 访问 产品对比指南
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)
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门