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等級
purum
品質等級
化驗
≥98.0% (GC)
形狀
liquid
折射率
n20/D 1.548 (lit.)
n20/D 1.548
bp
110-113 °C/0.5 mmHg (lit.)
密度
1.189 g/mL at 25 °C (lit.)
官能基
sulfone
儲存溫度
2-8°C
SMILES 字串
C=CCS(=O)(=O)c1ccccc1
InChI
1S/C9H10O2S/c1-2-8-12(10,11)9-6-4-3-5-7-9/h2-7H,1,8H2
InChI 密鑰
KYPIULIVYSQNNT-UHFFFAOYSA-N
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應用
Possible usages of allyl phenyl sulfone:
- It can undergo isomerization by the nonionic proazaphosphatrane catalysts under mild reaction conditions.
- It can react with epoxymesylate to give cycloalkane derivative. This method has been employed in the synthesis of marine eicosanoid bacillariolides I-III.
- It can undergo electrocatalytic additions to vinyl sulfones catalyzed by an electrogenerated base.
Starting material for the preparation of 1-alkyl-2-methylethenes; Michael additions to enones; Synthesis of α,β-unsaturated nitriles
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
235.4 °F - closed cup
閃點(°C)
113 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Highly efficient, catalytic bis addition reactions of allyl phenyl sulfone to vinyl sulfones.
Tetrahedron Letters, 45(25), 4841-4845 (2004)
One-Pot Synthesis of Cycloalkane Derivatives using Allyl Phenyl Sulfone and Epoxymesylate.
Tetrahedron, 56(41), 8077-8081 (2000)
The Journal of Organic Chemistry, 46, 4817-4817 (1981)
Journal of the Chemical Society. Perkin Transactions 1, 123-123 (1977)
Tetrahedron Letters, 22, 1905-1905 (1981)
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