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2 L
¥9,275.82
About This Item
经验公式（希尔记法）:
BBr3
CAS号:
分子量:
250.52
MDL编号:
UNSPSC代码:
12352101
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
表单
liquid
质量水平
浓度
1.0 M in methylene chloride
密度
1.467 g/mL at 25 °C
SMILES字符串
BrB(Br)Br
InChI
1S/BBr3/c2-1(3)4
InChI key
ILAHWRKJUDSMFH-UHFFFAOYSA-N
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此商品 | 211230 | 403857 | 202207 |
|---|---|---|---|
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| density 1.467 g/mL at 25 °C | density 0.859 g/mL at 25 °C | density 0.869 g/mL at 25 °C | density 2.60 g/mL at 20 °C (lit.) |
| form liquid | form liquid | form liquid | form - |
| concentration 1.0 M in methylene chloride | concentration 1.0 M in hexanes | concentration 1.0 M in heptane | concentration - |
一般描述
三溴化硼（BBr3）是有机化学中常用的去甲基试剂。[1]
应用
作为反应物用于制备：
- 药物中间体 6-硝基-L-多巴
- 带有空间保护的咔唑硼烷基团的发光聚苯乙烯衍生物
- 通过 Wurtz 型还原偶联反应得到高质量的硼掺杂石墨烯
- 巯基 (+)-甲基苯丙胺半抗原合成提高表位密度的 (+)-甲基苯丙胺结合疫苗
- 微米级有机分子-DNA 杂化结构
- 亲电芳香硼化反应合成硼烷配合物
- 5-HT2C 受体激动剂
- 具有叔氨基的联苯衍生物作为 ß-分泌酶 (BACE1) 抑制剂治疗阿尔茨海默病
- 高近红外区荧光 p-延伸的硼氮杂双吡咯亚甲基基团单元
- 甲氧基取代的 N-苯乙基酰亚胺分子内环化合成四氢异喹啉衍生物
在从香豆素支架合成苯并吡喃苯并吡喃的过程中用于裂解芳基甲基醚。[2]
包装
建议将25 mL Sure/Seal™ 瓶作为一次性瓶使用。 反复穿刺可能导致产品性能下降。
法律信息
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
警示用语：
Danger
危险分类
Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
靶器官
Central nervous system
储存分类代码
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Azobenzene derivatives show anti-cancer activity against pancreatic cancer cells only under nutrient starvation conditions via G0/G1 cell cycle arrest
Shinzawa K, et al.
Tetrahedron, 85, 132077-132077 (2021)
Tetrahedron Letters, 47, 5909-5909 (2006)
Hui Wang et al.
European journal of medicinal chemistry, 88, 66-73 (2014-09-14)
The pharmacokinetics (PK) and pharmacodynamics (PD) of PT119, a potent Staphylococcus aureus enoyl-ACP reductase (saFabI) inhibitor with a Ki value of 0.01 nM and a residence time of 750 min on the enzyme target, has been evaluated in mice. PT119
Andrey S Mereshchenko et al.
Nature chemistry, 7(7), 562-568 (2015-06-24)
'Roaming' is a new and unusual class of reaction mechanism that has recently been discovered in unimolecular dissociation reactions of isolated molecules in the gas phase. It is characterized by frustrated bond cleavage, after which the two incipient fragments 'roam'
Doriane Lorendeau et al.
Biochemical pharmacology, 90(3), 235-245 (2014-05-31)
The multidrug resistance protein 1 (MRP1) is involved in multidrug resistance of cancer cells by mediating drug efflux out of cells, often in co-transport with glutathione (GSH). GSH efflux mediated by MRP1 can be stimulated by verapamil. In cells overexpressing
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