推荐产品
质量水平
检测方案
98%
折射率
n20/D 1.426 (lit.)
bp
152 °C (lit.)
密度
0.97 g/mL at 25 °C (lit.)
SMILES字符串
CON(C)C(C)=O
InChI
1S/C4H9NO2/c1-4(6)5(2)7-3/h1-3H3
InChI key
OYVXVLSZQHSNDK-UHFFFAOYSA-N
一般描述
简单的 Weinreb 酰胺用于合成海洋天然产物 myriaporone 和usneoidone 作为酮合成子。
警示用语：
Warning
危险声明
危险分类
Flam. Liq. 3
WGK
WGK 3
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
European Journal of Organic Chemistry, 9, 1911-1922 (2004)
Asymmetric synthesis of heterocycles using sulfinimines (N-sulfinyl imines).
Davis FA, et al.
ARKIVOC (Gainesville, FL, United States), 7, 120-128 (2006)
Total synthesis of natural myriaporones.
Marta Pérez et al.
Angewandte Chemie (International ed. in English), 43(13), 1724-1727 (2004-03-24)
Xue Zhi Zhao et al.
Bioorganic & medicinal chemistry, 14(23), 7816-7825 (2006-08-16)
The diketo acid (DKA) class of HIV-1 integrase inhibitors are thought to function by chelating divalent metal ions within the enzyme catalytic center. However, differences in mutations conferring resistance among sub-families of DKA inhibitors suggest that multiple binding orientations may
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