推荐产品
品質等級
化驗
≥95.0%
95%
形狀
crystals
mp
284-288 °C (lit.)
SMILES 字串
OB(O)c1ccc(Br)cc1
InChI
1S/C6H6BBrO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI 密鑰
QBLFZIBJXUQVRF-UHFFFAOYSA-N
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應用
试剂用于
试剂用于制备
- 钯催化 Suzuki-Miyaura 交叉偶联
- 钯(II)催化的非对映选择性共轭加成
- 钯催化烯丙基酯与芳基硼酸的立体选择性 Heck 型反应
- 串联型Pd(II)催化的氧化Heck反应和分子内C-H酰胺化序列
- 铜介导芳基硼酸与氟烷基碘的无连接有氧氟烷基化反应
- Pd催化炔烃的碳钯化芳基环化炔烃或烯酮
- 铜催化的交叉耦合
试剂用于制备
- 具有潜在抗肿瘤活性的含没食子酸酯的 obovatol 类似物
- 蛋白调节剂、酶抑制剂和激酶抑制剂
其他說明
含不定量的酸酐
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
James A Jordan-Hore et al.
Organic letters, 14(10), 2508-2511 (2012-05-02)
Ligand-free cationic Pd(II) catalyst with NaNO3 as an additive is a highly active catalytic system for conjugate additions to sterically hindered γ-substituted cyclohexenones. More challenging γγ- and βγ-substrates also react well to produce products with quaternary centers in good dr.
Synthesis of obovatol derivatives and their preliminary evaluation as antitumor agents
Lee, M.-S.; et al.
Bull. Korean Chem. Soc., 28, 1601-1604 (2007)
Jingyi Ye et al.
International journal of nanomedicine, 14, 5623-5636 (2019-08-24)
The objective of this study was to compare the in vitro Fick's first law, in vitro lipolysis, and in vivo rat assays for oral absorption of Biopharmaceutical Classification Systems Class II (BCS II) drugs in self-nanoemulsifying drug delivery system (SNEDDS)
Tahlia R Meola et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 129, 145-153 (2018-06-02)
The synergistic effect of nanosizing and lipid-based drug delivery systems (LBDDS) was explored to enhance formulation drug loading levels and improve drug solubilisation in the gastrointestinal environment. A novel formulation combining drug nanocrystals and silica-lipid hybrid (SLH) microparticles as a
Chuan Xiao et al.
Bioorganic & medicinal chemistry, 19(23), 7100-7110 (2011-11-01)
A series of purine nucleoside analogues bearing an aryl and hetaryl group in position 6 were prepared and their biological activities were assessed by in vitro CDK1/Cyclin B1 and CDK2/Cyclin A2 kinase assay. From the synthesized chemicals, three Xylocydine derivatives
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