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品質等級
化驗
≥98%
顏色
colorless to faint yellow
密度
0.92 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
CC(C)CC(=O)CC(C)=O
InChI
1S/C8H14O2/c1-6(2)4-8(10)5-7(3)9/h6H,4-5H2,1-3H3
InChI 密鑰
IGMOYJSFRIASIE-UHFFFAOYSA-N
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應用
Reactant involved in:
- Cyclocondensation and deacetylation of dibromo(phenylsulfonyl)propene derivatives for synthesis of disubstituted furans
- Synthesis of dual activity effectors of angiotensin II type 1 receptors and peroxisome proliferator-activated receptor-γ
- Addition reactions with 1-alkynes
- Knoevenagel condensation
- Oxidative free radical reactions with 2-amino-1,4-benzoquinones
- Mild oxidative cleavage for synthesis of carboxylic acids
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
138.2 °F - closed cup
閃點（°C）
59 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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文章
Knoevenagel Condensation 是以 Emil Knoevenagel 命名的有機反應。它是典型的 C-C 鍵形成反應，也是 Aldol Condensation 的改良。
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
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