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Merck
CN

06061

Sigma-Aldrich

烯丙基苯砜

purum, ≥98.0% (GC)

别名:

(2-Propen-1-ylsulfonyl)benzene, (2-Propenylsulfonyl)benzene, (Allylsulfonyl)benzene, Phenyl 2-propenyl sulfone

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About This Item

线性分子式:
C6H5SO2CH2CH=CH2
CAS号:
分子量:
182.24
Beilstein:
1863561
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

purum

质量水平

方案

≥98.0% (GC)

表单

liquid

折射率

n20/D 1.548 (lit.)
n20/D 1.548

沸点

110-113 °C/0.5 mmHg (lit.)

密度

1.189 g/mL at 25 °C (lit.)

官能团

sulfone

储存温度

2-8°C

SMILES字符串

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 key

KYPIULIVYSQNNT-UHFFFAOYSA-N

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应用

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
M. Hirama
Tetrahedron Letters, 22, 1905-1905 (1981)
D. Savoia et al.
Journal of the Chemical Society. Perkin Transactions 1, 123-123 (1977)
D.F. Taber et al.
The Journal of Organic Chemistry, 46, 4817-4817 (1981)

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