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质量水平
方案
99%
表单
solid
mp
121-124 °C (lit.)
SMILES字符串
O[Se](=O)c1ccccc1
InChI
1S/C6H6O2Se/c7-9(8)6-4-2-1-3-5-6/h1-5H,(H,7,8)
InChI key
WIHKGDVGLJJAMC-UHFFFAOYSA-N
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一般描述
Benzeneseleninic acid oxidizes hydrazine or 1,2-disubstituted derivatives to corresponding diazenes.
应用
Benzeneseleninic acid was used as catalyst during the oxidation of sulfides to sulfoxides via ligand coupling on the iodine atom. It was also used in the preparation of 3-methoxy-17a-oxa-D-homoestra-l,3,5(10)-trien-17-one.
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 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Oxidation of hydrazines with benzeneseleninic acid and anhydride.
Back TG, et al.
The Journal of Organic Chemistry, 46(8), 1564-1570 (1981)
Facile oxidation of sulfides to sulfoxides using iodosobenzene and benzeneseleninic acid as a catalyst.
Roh KR, et al.
Tetrahedron Letters, 32(6), 793-796 (1991)
1, 2-Hydrogen shifts in thermal and photic Bamford-Stevens reactions of cyclohexanones. Activation by an endocyclic oxygen.
Olmstead KK and Nickon A.
Tetrahedron, 54(40), 12161-12172 (1998)
Craig A Bayse
Journal of inorganic biochemistry, 104(1), 1-8 (2009-10-30)
The toxicity of selenium is a major barrier to its application to the prevention of cancer, cardiovascular disease, and other chronic ailments. Organic seleninic acids, as well as other reducible selenium compounds, have been shown to react with biological sulfhydryls
S Zheng et al.
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao, 26(4), 371-374 (1995-12-01)
In view of the negative relationship between selenium and cancer, we designed and synthesized eleven substituted benzeneselenic acids (IVa-k) The antineoplastic activity of the title compounds was evaluated via the tests of inhibition of acetylcholinesterase, HL-60 and K562 in vitro
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