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Merck

375152

Sigma-Aldrich

苯硒酚

97%

别名:

硒酚, 苯基硒硫醇, 苯基硒酚

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About This Item

线性分子式:
C6H5SeH
CAS号:
分子量:
157.07
Beilstein:
385715
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

liquid

折射率

n20/D 1.616 (lit.)

bp

71-72 °C/18 mmHg (lit.)

密度

1.479 g/mL at 25 °C (lit.)

SMILES 字串

[SeH]c1ccccc1

InChI

1S/C6H6Se/c7-6-4-2-1-3-5-6/h1-5,7H

InChI 密鑰

WDODWFPDZYSKIA-UHFFFAOYSA-N

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一般說明

苯硒醇是一种芳基硒醇。本文报道了二苯基二硒醚在钨灯照射下能促进苯硒醇自由基加成到灭活的乙炔上。报道了苯乙烯醇催化锡烷介导的自由基链反应,通过二苯基二硒醚与氢化三丁基锡的还原反应原位生成。

應用

在单烯烃基取代的1,3-二烯的合成中,苯砜可以用作起始试剂。可用于合成阳离子硫醇桥联二钌配合物。

訊號詞

Danger

危險分類

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

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

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Lorenzo Maserati et al.
Nanoscale, 13(1), 233-241 (2020-12-18)
Hybrid quantum wells are electronic structures where charge carriers are confined along stacked inorganic planes, separated by insulating organic moieties. 2D quantum-confined hybrid materials are of great interest from a solid-state physics standpoint because of the rich many-body phenomena they
Diphenyl diselenide-promoted radical addition of benzeneselenol to acetylenes.
Ogawa A, et al.
Tetrahedron Letters, 33(10), 1329-1332 (1992)
David Crich et al.
Accounts of chemical research, 40(6), 453-463 (2007-05-11)
The discovery and development of the catalysis of stannane-mediated radical chain reactions by benzeneselenol, generated in situ by reduction of diphenyl diselenide with tributyltin hydride, are described. The catalytic sequence is discussed in terms of polarity reversal catalysis of radical
Justin P Johnpeter et al.
Inorganic chemistry, 52(23), 13663-13673 (2013-11-20)
A series of cationic chalcogenolato-bridged diruthenium complexes [(η(6)-p-MeC6H4Pr(i))2Ru2(μ-EC6H5)3](+) (E = S, 1; E = Se, 2; E = Te, 3) has been obtained in ethanol from the reaction of (η(6)-p-MeC6H4Pr(i))2Ru2(μ-Cl)2Cl2 with benzenethiol, benzeneselenol, and sodium tellurophenolate, respectively. The thiolato and
Nikolay V Orlov et al.
The Journal of organic chemistry, 79(24), 12111-12121 (2014-10-08)
A unique Ni-catalyzed transformation is reported for the one-pot highly selective synthesis of previously unknown monoseleno-substituted 1,3-dienes starting from easily available terminal alkynes and benzeneselenol. The combination of a readily available catalyst precursor, Ni(acac)2, and an appropriately tuned phosphine ligand

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