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关于此项目
线性分子式:
C6H5SO2CH2CH=CH2
化学文摘社编号:
分子量:
182.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
240-338-8
Beilstein/REAXYS Number:
1863561
MDL number:
Assay:
≥98.0% (GC)
Form:
liquid
grade
purum
Quality Level
assay
≥98.0% (GC)
form
liquid
refractive index
n20/D 1.548
bp
110-113 °C/0.5 mmHg (lit.)
density
1.189 g/mL at 25 °C (lit.)
functional group
sulfone
storage temp.
2-8°C
SMILES string
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 key
KYPIULIVYSQNNT-UHFFFAOYSA-N
Application
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
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
M. Hirama
Tetrahedron Letters, 22, 1905-1905 (1981)
Proazaphosphatrane P (RNCH2CH2) 3N (R= Me, i?Pr)?Catalyzed Isomerization of Allylaromatics, Allyl Phenyl Sulfide, Allyl Phenyl Sulfone, and bis?Allylmethylene Double Bond?Containing Compounds
Yu Z, et al.
Advanced Synthesis & Catalysis, 348(1?2), 111-117 (2006)
One-Pot Synthesis of Cycloalkane Derivatives using Allyl Phenyl Sulfone and Epoxymesylate.
Miyaoka H, et al.
Tetrahedron, 56(41), 8077-8081 (2000)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 143847-10G | 04061838735188 |
| 143847-50G | 04061838735195 |
| 06061-50ML | 04061837253805 |
| 06061-10ML | 04061837253799 |
