243965
苯基溴化硒
98%
别名:
Benzeneselenyl bromide, 苯硒基溴化物
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线性分子式:
C6H5SeBr
化学文摘社编号:
分子量:
235.97
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
252-238-1
Beilstein/REAXYS Number:
2039772
MDL number:
Assay:
98%
Form:
solid
产品名称
苯基溴化硒, 98%
form
solid
InChI key
LCEFEIBEOBPPSJ-UHFFFAOYSA-N
InChI
1S/C6H5BrSe/c7-8-6-4-2-1-3-5-6/h1-5H
SMILES string
Br[Se]c1ccccc1
assay
98%
bp
107-108 °C/15 mmHg (lit.)
mp
58-62 °C (lit.)
Quality Level
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Application
苯硒基溴被用于制备 exo -2-甲基-7-苯基硒基-八氢-8-氧杂-2,7 b -二氮杂-双环戊酮 [ a , e 戊烯-1,3-二酮和 endo -2-甲基-7-苯基硒酰-八氢-8-氧杂-2,7 b -二氮杂-双环戊酮[ a , e ] 戊烯-1,3-二酮 。也用于 α-硒烯化合成烯酮-氰基酮与萘锂 。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Met. Corr. 1 - STOT RE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
X= Y?ZH Systems as potential 1, 3-dipoles. Part 52: Fused-ring forming electrophile induced oxime→nitrone→ cycloaddition cascades.
Ali Dondas H, et al.
Tetrahedron Letters, 57(32), 7035-7045 (2001)
Synlett, 1274-1274 (2007)
Santanu Hati et al.
European journal of medicinal chemistry, 100, 188-196 (2015-06-19)
Herein we have reported design, synthesis and in vitro biological evaluation of a library of bicyclic lactams that led to the discovery of compounds 6 and 7 as a novel class of α-glucosidase inhibitors. They inhibited α-glucosidase (yeast origin) in a
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