추천 제품
vapor pressure
1 hPa ( 748 °C)
제품 라인
ReagentPlus®
분석
≥99%
형태
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
LiBr/Chlorotrimethylsilane reagent participates in the conversion of alcohols to bromides.
애플리케이션
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).
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
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)
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)
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)
Eoghan M Cunnane et al.
ACS applied materials & interfaces, 12(24), 26955-26965 (2020-05-23)
Vascular tissue engineering is aimed at developing regenerative vascular grafts to restore tissue function by bypassing or replacing defective arterial segments with tubular biodegradable scaffolds. Scaffolds are often combined with stem or progenitor cells to prevent acute thrombosis and initiate
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