所有图片(1)
About This Item
经验公式（希尔记法）:
C4H4BrNO2
CAS号:
分子量:
177.98
MDL编号:
UNSPSC代码:
12352115
EC索引号:
204-877-2
NACRES:
NA.22
产品名称
N-Bromosuccinimide, for synthesis
蒸汽压
14.8 hPa ( 20 °C)
质量水平
表单
powder
效能
>2000 mg/kg LD50, oral (Rat)
反应适用性
reagent type: oxidant
mp
174-179 °C
溶解性
14.8 g/L (decomposition)
密度
2.1 g/cm3 at 20 °C
堆积密度
750 kg/m3
储存温度
2-8°C
SMILES字符串
BrN1C(=O)CCC1=O
InChI
1S/C4H4BrNO2/c5-6-3(7)1-2-4(6)8/h1-2H2
InChI key
PCLIMKBDDGJMGD-UHFFFAOYSA-N
应用
- Mechanistic study on iodine-catalyzed aromatic bromination of aryl ethers by N-bromosuccinimide: This study explores the roles of NBS in organic synthesis, particularly in radical and electrophilic substitutions (Pramanick et al., 2017).
- One‐Pot Protocol for the Synthesis of Imidazoles and Quinoxalines using N‐Bromosuccinimide: This paper reports a green, efficient synthesis of heterocycles mediated by NBS (Pardeshi et al., 2017).
- N-Bromosuccinimide as an Interfacial Alleviator for Br/I Exchange in Perovskite for Solar Cell Fabrication: This research demonstrates the use of NBS in improving the crystallization and defect passivation in perovskite solar cells (Pegu et al., 2021).
- N‐Bromosuccinimide‐Mediated Radical Cyclization of 3‐Arylallyl Azides: Synthesis of 3‐Substituted Quinolines: Discusses the application of NBS under visible light irradiation to synthesize quinolines (Wang et al., 2015).
- N-Bromosuccinimide mediated synthesis of triazatruxenes from indoles: This study highlights the cyclotrimerization of indoles using NBS, demonstrating its utility as a reagent in complex organic transformations (Toworakajohnkun et al., 2017).
分析说明
Assay (iodometric): ≥ 99.0 %
Identity (IR): passes test
Identity (IR): passes test
警示用语：
Warning
危险分类
Aquatic Acute 1 - Eye Irrit. 2 - Met. Corr. 1 - Muta. 2 - Ox. Sol. 3 - Skin Irrit. 2 - Skin Sens. 1B
储存分类代码
5.1B - Oxidizing hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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