추천 제품
Grade
ACS reagent
vapor density
7.14 (vs air)
vapor pressure
175 mmHg ( 20 °C)
671 mmHg ( 55 °C)
분석
≥99.5%
형태
liquid
저항도
7.8E18 μΩ-cm, 20°C
불순물
organic bromine compounds, passes test
≤0.001% I2
≤0.001% S compounds
증발 잔류물
≤0.005%
bp
58.8 °C (lit.)
mp
−7.2 °C (lit.)
density
3.119 g/mL at 25 °C (lit.)
음이온 미량물
chloride (Cl-): ≤0.05%
양이온 미량물
Ni: ≤5 ppm
heavy metals: ≤2 ppm
SMILES string
BrBr
InChI
1S/Br2/c1-2
InChI key
GDTBXPJZTBHREO-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Bromine is a highly volatile and reactive halogen that can be used as a powerful brominating and oxidizing agent in chemical synthesis.
애플리케이션
Bromine can be used as a brominating agent for the bromination of:
It can also be used as an oxidizing agent for the oxidation of:
It can also be used as a Lewis acid catalyst to:
- Aromatic and heterocyclic compounds.
- Carbonyl compounds at α position to carbonyl groups.
- Aromatic carboxylic acids via Hell-Volhard-Zelinski reaction in the presence of phosphorus trihalides.
- Alkylbenzenes at the benzylic position using photocatalytic conditions.
It can also be used as an oxidizing agent for the oxidation of:
- Primary alcohols to either aldehydes or esters.
- Secondary alcohols to ketones.
It can also be used as a Lewis acid catalyst to:
- Convert epoxides and CO2 to cyclic carbonates in a continuous flow system.
- Synthesize bis(indolyl)methanes by reacting indoles with carbonyl compounds.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A
Storage Class Code
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
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.
Reaction of bromine and chlorine with phenolic compounds and natural organic matter extracts-Electrophilic aromatic substitution and oxidation.
Criquet J, et al.
Water Research, 85, 476-486 (2015)
Bromine-catalyzed aziridination of olefins. A rare example of atom-transfer redox catalysis by a main group element.
Jeong JUK, et al.
Journal of the American Chemical Society, 120(27), 6844-6845 (1998)
Jennifer A Kozak et al.
Journal of the American Chemical Society, 135(49), 18497-18501 (2013-11-22)
A continuous method for the formation of cyclic carbonates from epoxides and carbon dioxide (CO2) is described. The catalysts used are inexpensive and effective in converting the reagents to the products in a residence time (t(R)) of 30 min. The
The chemistry of atmospheric bromine.
Wofsy SC, et al.
Geophysical Research Letters, 2(6), 215-218 (1975)
Nickel-butadiene catalytic system for the cross-coupling of bromoalkanoic acids with alkyl Grignard reagents: a practical and versatile method for preparing fatty acids.
Takanori Iwasaki et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(9), 2956-2960 (2013-02-02)
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