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品質等級
化驗
97%
形狀
solid
mp
57-64 °C
官能基
ketone
SMILES 字串
C[C@]12CCC(=O)C=C1CCC2=O
InChI
1S/C10H12O2/c1-10-5-4-8(11)6-7(10)2-3-9(10)12/h6H,2-5H2,1H3/t10-/m0/s1
InChI 密鑰
FNYAZSZTENLTRT-JTQLQIEISA-N
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應用
(S)-(+)-Hajos-Parrish diketone can be used as a reactant in:
- The total synthesis of steroidal alkaloids cortistatins.
- The stereoselective preparation of hydroanthracenol and related polycyclic compounds via Ti(Oi-Pr)4-promoted photoenolization Diels-Alder reaction.
- The synthesis of γ,γ-disubstituted allyldiboron compounds by reacting with allylic 1,1-diboronate reagents via Cu-catalyzed borylation and 1,2-addition reaction.
訊號詞
Danger
危險分類
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
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
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Singlet oxygen-mediated selective C--H bond hydroperoxidation of ethereal hydrocarbons
Nature Communications, 8(1), 1-8 (2017)
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