449873
Bromuro de litio
AnhydroBeads™, −10 mesh, ≥99.9% trace metals basis
Sinónimos:
Lithium monobromide
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Fórmula lineal:
LiBr
Número CAS:
Peso molecular:
86.85
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-439-8
MDL number:
Assay:
≥99.9% trace metals basis
Grade:
synthesis grade
Servicio técnico
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Permítanos ayudarlegrade
synthesis grade
product line
AnhydroBeads™
assay
≥99.9% trace metals basis
reaction suitability
core: lithium
impurities
≤1000.0 ppm Trace Metal Analysis
particle size
−10 mesh
mp
550 °C (lit.)
application(s)
battery precursors
catalysts
material synthesis precursor
SMILES string
[Li+].[Br-]
InChI
1S/BrH.Li/h1H;/q;+1/p-1
InChI key
AMXOYNBUYSYVKV-UHFFFAOYSA-M
Legal Information
AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 2
flash_point_f
No data available
flash_point_c
No data available
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Zhongli Cai et al.
Radiation research, 159(3), 411-419 (2003-02-26)
An investigation of electron and hole transfer to oxidized guanine bases in DNA is reported. Guanine in DNA was preferentially oxidized by Br(2)(*-) at 298 K to 8-oxo-7,8-dihydro-guanine (8-oxo-G) and higher oxidation products. HPLC-EC analysis of irradiated DNA shows that
R Quaderer et al.
Organic letters, 3(20), 3181-3184 (2001-09-28)
[reaction: see text] The alkanesulfonamide "safety-catch" resin has proven useful for Fmoc-based synthesis of C-terminal peptide thioesters. We now report that the yield of isolated thioester can increase significantly when the cleavage reaction is carried out in 2 M LiBr/THF
Arlette Solladié-Cavallo et al.
The Journal of organic chemistry, 70(5), 1605-1611 (2005-02-26)
Both symmetrical and nonsymmetrical trans-2,3-diaryloxiranes are regio- and stereoselectively opened by the LiBr/Amberlyst 15 system. In the case of symmetrical trans-stilbene oxide, the syn- versus anti-bromohydrins ratio ranged between 88/12 and 30/70, by varying the reaction temperature from 20 to