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关于此项目
线性分子式:
O2NC6H4SeCN
化学文摘社编号:
分子量:
227.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
257-350-4
Beilstein/REAXYS Number:
1309777
MDL number:
Assay:
97.5%
Quality Level
assay
97.5%
mp
140-142 °C (lit.)
functional group
nitro
SMILES string
[O-][N+](=O)c1ccccc1[Se]C#N
InChI
1S/C7H4N2O2Se/c8-5-12-7-4-2-1-3-6(7)9(10)11/h1-4H
InChI key
LHBLJWULWKQRON-UHFFFAOYSA-N
General description
2-硝基苯基硒氰酸酯是一种发色团硒化合物。
Application
可使用 2-硝基苯基硒氰酸酯( o -硝基苯基硒氰酸酯):
- 研究其与金属硫蛋白锌/硫醇盐簇发生反应的机制
- 2,3-开环-5α-胆甾烷-2,3-二醇制备过程中
- 4α-甲基-2,3-开环-5α-胆甾烷-2,3-二醇制备过程中
- 2-硝基苯硒基衍生物制备过程中
- 3α-[(2-硝基苯基)硒] 雄甾-1,5-二烯-17β-ol合成过程中
signalword
Danger
hcodes
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
Synthesis and radical oxidation of steroidal 1-oxo-5α-alcohols.
Khripach VA, et al.
ARKIVOC (Gainesville, FL, United States), 9, 20-28 (2008)
M Arnó et al.
Steroids, 43(3), 305-314 (1984-03-01)
The reaction of 2,3-seco-5 alpha-cholestane-2,3-diol and 4 alpha-methyl-2,3-seco-5 alpha-cholestane-2,3-diol with o-nitrophenyl selenocyanate was studied. The diols were synthesized from cholesterol.
Shaoman Zhou et al.
Journal of medicinal chemistry, 49(20), 6120-6128 (2006-09-29)
All stereoisomers of adenine and guanine methylene-3-fluoromethylenecyclopropane analogues of nucleosides 9a, 9b, 10a, 10b, 11a, 11b, 12a, and 12b were synthesized and their antiviral activities were evaluated. A highly convergent approach permitted the synthesis of all these analogues using a
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 365246-1G | 04061831825756 |


