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Merck
CN

243965

Phenylselenyl bromide

98%

Synonym(s):

Benzeneselenenyl bromide, Benzeneselenyl bromide

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About This Item

Linear Formula:
C6H5SeBr
CAS Number:
34837-55-3
Molecular Weight:
235.97
Beilstein:
2039772
EC Number:
252-238-1
MDL number:
MFCD00000047
UNSPSC Code:
12352100
PubChem Substance ID:
24854643
NACRES:
NA.22

Key Documents

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Quality Level

100

Assay

98%

form

solid

bp

107-108 °C/15 mmHg (lit.)

mp

58-62 °C (lit.)

SMILES string

Br[Se]c1ccccc1

InChI

1S/C6H5BrSe/c7-8-6-4-2-1-3-5-6/h1-5H

InChI key

LCEFEIBEOBPPSJ-UHFFFAOYSA-N

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Application

Phenylselenyl bromide was used in the preparation of exo-2-methyl-7-phenylselenyl-octahydro-8-oxa-2,7b-diaza-dicyclopenta[a,e]pentalene-1,3-dione and endo-2-methyl-7-phenylselanyl-octahydro-8-oxa-2,7b-diaza-dicyclopenta[a,e]pentalene-1,3-dione. It was also used in the synthesis of enones by selenenylation of α-cyano ketones with lithium naphthalenide.

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR6316
MKCL3339
MKCB2590V
MKBT6821V
MKBP3058V

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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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