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化驗
97%
形狀
liquid
折射率
n20/D 1.488 (lit.)
bp
74 °C/15 mmHg (lit.)
mp
3-5 °C (lit.)
密度
0.980 g/mL at 20 °C
0.971 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
CC1=CC(=O)CC1
InChI
1S/C6H8O/c1-5-2-3-6(7)4-5/h4H,2-3H2,1H3
InChI 密鑰
CHCCBPDEADMNCI-UHFFFAOYSA-N
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一般說明
3-Methyl-2-cyclopentenone undergoes reduction in presence of triethylammonium formate and palladium catalyst to form saturated ketone. It undergoes B(C6F5)3 catalyzed hydrosilation to yield complex reaction mixtures of 1,2 addition products and oligomers.
應用
3-Methyl-2-cyclopentenone was used in the synthesis of 2-hydroxy-3-methyl-2-cyclopentenone.
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
149.0 °F - closed cup
閃點(°C)
65 °C - closed cup
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
其他客户在看
Palladium-catalyzed reductions of. alpha.,. beta.-unsaturated carbonyl compounds, conjugated dienes, and acetylenes with trialkylammonium formates.
The Journal of Organic Chemistry, 43(20), 3985-3987 (1978)
A new synthesis of cyclopentenones: dihydrojasmone.
The Journal of Organic Chemistry, 50(12), 2110-2112 (1985)
B(C6F5)3 catalyzed hydrosilation of enones and silyl enol ethers.
Tetrahedron, 58(41), 8247-8254 (2002)
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