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Merck
CN

213365

Sigma-Aldrich

二氧化硒

ReagentPlus®, powder, 99.8% trace metals basis

别名:

NSC 56753, 氧化硒

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About This Item

线性分子式:
SeO2
CAS号:
分子量:
110.96
EC 号:
MDL编号:
UNSPSC代码:
12352303
PubChem化学物质编号:
NACRES:
NA.23

蒸汽压

1 mmHg ( 157 °C)

质量水平

产品线

ReagentPlus®

方案

99.8% trace metals basis

表单

powder

颜色

white

mp

315 °C (subl.) (lit.)

SMILES字符串

O=[Se]=O

InChI

1S/O2Se/c1-3-2

InChI key

JPJALAQPGMAKDF-UHFFFAOYSA-N

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应用

烯丙基烯烃和炔烃的温和氧化剂。可将 1,3-二酮转化为 1,2,3-三酮。

其他说明

Material may contain dark crystals which are unavoidable and do not impact product quality

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

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

储存分类代码

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

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Asian Journal of Chemistry, 19, 4107-4107 (2007)
Tetrahedron Letters, 34, 2979-2979 (1993)
Haiying Luo et al.
Colloids and surfaces. B, Biointerfaces, 94, 304-308 (2012-03-02)
In vitro antiproliferative effects of selenium nanoparticles (nanoSe(0), 10-40 μmol/L) on HeLa (human cervical carcinoma) cells and MDA-MB-231 (human breast carcinoma) cells were examined by optical microscopic inspection and MTT assay in the present study. The nanoSe(0) effectively inhibited the
Mojtaba Shakibaie et al.
Pharmaceutical biology, 51(1), 58-63 (2012-10-06)
In the present investigation, acute and subacute toxicity of the biogenic Se nanoparticles (Se NPs) has been reported. To characterize the Se NPs produced by a bacterium species and to evaluate their toxicity and impact on clinical chemistry and hematological
Erik A A Wallén et al.
Organic letters, 9(3), 389-391 (2007-01-26)
[reaction: see text] An efficient synthetic route to Cbz-protected 3-aminomethyl-2-aryl-8-bromo-6-chlorochromones has been developed. 3-Aryl-1-(3-bromo-5-chloro-2-hydroxyphenyl)-2-propen-1-one or 2-aryl-8-bromo-6-chlorochroman-4-one could be reacted under Mannich conditions yielding 2-aryl-8-bromo-6-chloro-3-methylenechroman-4-one, which was further converted to the target compound via an aza-Michael reaction followed by an SeO(2)

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