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About This Item
Linear Formula:
LiBr
CAS Number:
Molecular Weight:
86.85
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21
vapor pressure
1 hPa ( 748 °C)
Quality Level
product line
ReagentPlus®
Assay
≥99%
form
powder
pH
7 (20 °C, 10 g/L)
mp
550 °C (lit.)
SMILES string
[Li+].[Br-]
InChI
1S/BrH.Li/h1H;/q;+1/p-1
InChI key
AMXOYNBUYSYVKV-UHFFFAOYSA-M
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General description
LiBr/Chlorotrimethylsilane reagent participates in the conversion of alcohols to bromides.
Application
Lithium bromide (LiBr) may be employed as a catalyst in the following studies:
- Transformation of (aromatic- and α,β-unsaturated) aldehydes to dithioacetals via solvent-free dithioacetalization.
- Synthesis of olefins via condensation reaction of carbonyl compounds with active methylene compounds.
- Green synthesis of β-amino alcohols.
- Chemo- and regioselective bromination of aromatic compounds was carried out by employing LiBr/ceric ammonium nitrate (CAN) reagent system (as a source of Br+ ion).
Other Notes
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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An efficient chemo and regioselective oxidative nuclear bromination of activated aromatic compounds using lithium bromide and ceric ammonium nitrate.
Roy SC, et al.
Tetrahedron Letters, 42(39), 6941-6942 (2001)
Lithium Bromide, an Inexpensive and Efficient Catalyst for Opening of Epoxide Rings by Amines at Room Temperature under Solvent-Free Condition.
Chakraborti AK, et al.
European Journal of Organic Chemistry, 2004(17), 3597-3600 (2004)
Lithium bromide as a new catalyst for carbon-carbon bond formation in the solid state.
Prajapati D, et al.
Journal of the Chemical Society. Perkin Transactions 1, 9, 959-960 (1996)
Lithium bromide-catalyzed highly chemoselective and efficient dithioacetalization of α,β-unsaturated and aromatic aldehydes under solvent-free conditions.
Firouzabadi H, et al.
Synthesis, 58-60 (1999)
Eoghan M Cunnane et al.
ACS applied materials & interfaces, 12(24), 26955-26965 (2020-05-23)
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