328057
4,4′-Dibromobenzil
90%, technical grade
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About This Item
Linear Formula:
BrC6H4COCOC6H4Br
CAS Number:
Molecular Weight:
368.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
252-628-1
MDL number:
Assay:
90%
InChI key
NYCBYBDDECLFPE-UHFFFAOYSA-N
InChI
1S/C14H8Br2O2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8H
SMILES string
Brc1ccc(cc1)C(=O)C(=O)c2ccc(Br)cc2
grade
technical grade
assay
90%
mp
224-226 °C (lit.)
functional group
bromo, ketone
Quality Level
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
Related Categories
Application
4,4′-Dibromobenzil was used in preparation of 5,5′-bis -(4-bromo-phenyl)-3-methyl-imidazolidine-2,4-dione, 5,5′- bis -(4-bromo-phenyl)-3-butyl-imidazolidine-2,4-dione, 5,5′-bis-(4-bromo-phenyl)-3-pentyl-imidazolidine-2,4-dione and 5,5′-bis -(4-chloro-phenyl)-3-ethyl imidazolidine-2,4-dione. It was also used in synthesis of novel quinoxaline-based sensitizers for dye-sensitized solar cells.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Dong Wook Chang et al.
Organic letters, 13(15), 3880-3883 (2011-06-28)
Novel quinoxaline-based organic sensitizers using vertical (RC-21) and horizontal (RC-22) conjugation between an electron-donating triphenylamine unit and electron-accepting quinoxaline unit have been synthesized and used for dye-sensitized solar cells (DSSCs), leading to the relatively high power conversion efficiencies of 3.30
A rapid and efficient microwave-assisted synthesis of hydantoins and thiohydantoins.
Muccioli GG, et al.
Tetrahedron, 59(8), 1301-1307 (2003)
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