推薦產品
等級
JIS special grade
蒸汽密度
7.14 (vs air)
蒸汽壓力
175 mmHg ( 20 °C)
671 mmHg ( 55 °C)
化驗
≥99.0%
形狀
liquid
存貨情形
available only in Japan
電阻係數
7.8E18 μΩ-cm, 20°C
bp
58.8 °C (lit.)
mp
−7.2 °C (lit.)
密度
3.119 g/mL at 25 °C (lit.)
SMILES 字串
BrBr
InChI
1S/Br2/c1-2
InChI 密鑰
GDTBXPJZTBHREO-UHFFFAOYSA-N
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訊號詞
Danger
危險分類
Acute Tox. 1 Inhalation - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1A
儲存類別代碼
6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Faceshields, Gloves, Goggles
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
Vitalij V Levin et al.
Organic letters, 15(4), 917-919 (2013-02-02)
Reactions of difluorocarbene with benzyl and alkylzinc halides leading to fluorinated organozinc species have been described. The generated α-difluorinated organozinc reagents are reasonably stable in solution and can be quenched with external electrophiles (iodine, bromine, proton), affording compounds containing the
Kimberly T Barrett et al.
Journal of the American Chemical Society, 135(8), 2963-2966 (2013-02-16)
We report the enantioselective synthesis of atropisomeric benzamides employing catalytic electrophilic aromatic substitution reactions involving bromination. The catalyst is a simple tetrapeptide bearing a tertiary amine that may function as a Brønsted base. A series of tri- and dibrominations were
John D Sivey et al.
Environmental science & technology, 47(3), 1330-1338 (2013-01-18)
HOBr, formed via oxidation of bromide by free available chlorine (FAC), is frequently assumed to be the sole species responsible for generating brominated disinfection byproducts (DBPs). Our studies reveal that BrCl, Br(2), BrOCl, and Br(2)O can also serve as brominating
Bromine-77 and iodine-123 radiopharmaceuticals.
G Stöcklin
The International journal of applied radiation and isotopes, 28(1-2), 131-147 (1977-01-01)
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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