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Merck
CN

213012

苯亚硒酸酐

70%

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关于此项目

线性分子式:
C6H5SeOOSeOC6H5
化学文摘社编号:
分子量:
360.13
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
2332406
MDL number:
Assay:
70%
Form:
powder
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SMILES string

O=[Se](O[Se](=O)c1ccccc1)c2ccccc2

InChI

1S/C12H10O3Se2/c13-16(11-7-3-1-4-8-11)15-17(14)12-9-5-2-6-10-12/h1-10H

InChI key

FHPZOWOEILXXBD-UHFFFAOYSA-N

assay

70%

form

powder

impurities

<30% benzeneseleninic acid

General description

苯硒酸酐氧化苯酚可产生 邻位-醌。苯硒酸酐可作为温和的氧化剂,用于将苄基烃转化为醛或酮

Application

用苯甲烯酐酸酐可通过氧化肼得到偶氮化合物

signalword

Danger

Hazard Classifications

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

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Comparative oxidation of phenols with benzeneseleninic anhydride and with benzeneseleninic acid.
Barton DHR, et al.
Tetrahedron, 44(20), 6397-6406 (1988)
Dehydrogenation of hydrazines and of 4-azacholestan-3-one with benzeneseleninic acid and benzeneseleninic anhydride.
Back TG.
Journal of the Chemical Society. Chemical Communications, 6, 278-279 (1978)
T Iida et al.
Journal of lipid research, 29(8), 1097-1101 (1988-08-01)
A facile one-step conversion of stereoisomeric methyl 3-hydroxycholanoates to 1,4-dien-3-one, by treatment in boiling toluene with iodoxybenzene catalyzed by benzeneselenic anhydride, is described. The direct oxidation-dehydrogenation at C-3 is applicable to other cholanoates (hyodeoxycholic, chenodeoxycholic, ursodeoxycholic, deoxycholic, and cholic) when
Naotoshi Toki et al.
Chemical & pharmaceutical bulletin, 52(8), 1009-1012 (2004-08-12)
Benzeneseleninic anhydride in the presence of tert-butyl hydroperoxide in chlorobenzene at about 70 degrees C is an effective oxidizing agent for the selective oxidation of alcohols at the benzylic position.
Preparation of aldehydes and ketones by oxidation of benzylic hydrocarbons with benzeneseleninic anhydride.
Barton DHR, et al.
Tetrahedron Letters, 20(35), 3331-3334 (1979)

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