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品質等級
化驗
98%
折射率
n20/D 1.426 (lit.)
bp
152 °C (lit.)
密度
0.97 g/mL at 25 °C (lit.)
SMILES 字串
CON(C)C(C)=O
InChI
1S/C4H9NO2/c1-4(6)5(2)7-3/h1-3H3
InChI 密鑰
OYVXVLSZQHSNDK-UHFFFAOYSA-N
一般說明
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。
訊號詞
Warning
危險聲明
危險分類
Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
120.2 °F - closed cup
閃點(°C)
49 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Total synthesis of natural myriaporones.
Angewandte Chemie (International ed. in English), 43(13), 1724-1727 (2004-03-24)
Asymmetric synthesis of heterocycles using sulfinimines (N-sulfinyl imines).
ARKIVOC (Gainesville, FL, United States), 7, 120-128 (2006)
European Journal of Organic Chemistry, 9, 1911-1922 (2004)
Acetylations of strongly basic and nucleophilic enolate anions with N-methoxy-N-methylacetamide.
Tetrahedron Letters, 24(18), 1851-1854 (1983)
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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