132756
1,2,4-Tribromobenzene
95%
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About This Item
Empirical Formula (Hill Notation):
C6H3Br3
CAS Number:
Molecular Weight:
314.80
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-433-9
MDL number:
Assay:
95%
Form:
solid
Quality Level
assay
95%
form
solid
mp
41-43 °C (lit.)
functional group
bromo
SMILES string
Brc1ccc(Br)c(Br)c1
InChI
1S/C6H3Br3/c7-4-1-2-5(8)6(9)3-4/h1-3H
InChI key
FWAJPSIPOULHHH-UHFFFAOYSA-N
General description
1,2,4-tribromobenzene on photochemical dehalogenation in open-air solutions of acetonitrile yields 1,4-dibromobenzene, 1,3-dibromobenzene and 1,2-dibromobenzene.
Application
1,2,4-tribromobenzene was used in the synthesis of hyperbranched poly(p-phenylene ethynylenes). It was used as cross-linking reagent during Pd-catalyzed cross-coupling of 2,5-diiodo-4-[(2-ethylhexyl)oxy]methoxybenzene and 1,4-diethynyl-2,5-bis-(octyloxy)benzene.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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E N Smith et al.
Journal of toxicology and environmental health, 6(4), 737-749 (1980-07-01)
1,2,4-Trichlorobenzene (TCB) and 1,2,4-tribromobenzene (TBB) were administered for 7 d to rats at a dose of 1 mmol/kg.d. The animals were sacrificed at various times to observe the decline in enzyme induction. Carbon 14-labeled TCB and TBB were administered and
Hyperbranched Poly (p-phenylene ethynylene) s.
Mendez JD, et al.
Macromolecular Chemistry and Physics, 208(15), 1625-1636 (2007)
Synthesis and characterization of cross-linked conjugated polymer milli-, micro-, and nanoparticles.
Eric Hittinger et al.
Angewandte Chemie (International ed. in English), 43(14), 1808-1811 (2004-04-01)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 132756-5G | 04061832684833 |