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10-Undecen-1-ol/十一烯醇 {[allProObj[0].p_purity_real_show]}

货号:A849391 同义名: 10-十一烯-1-醇

10-Undecen-1-ol, converted from ricinoleic acid, can be used as a comonomer for the introduction of functional groups .

10-Undecen-1-ol/十一烯醇 化学结构 CAS号:112-43-6
10-Undecen-1-ol/十一烯醇 化学结构
CAS号:112-43-6
10-Undecen-1-ol/十一烯醇 3D分子结构
CAS号:112-43-6
10-Undecen-1-ol/十一烯醇 化学结构 CAS号:112-43-6
10-Undecen-1-ol/十一烯醇 3D分子结构 CAS号:112-43-6
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10-Undecen-1-ol/十一烯醇 生物活性

描述 10-Undecen-1-ol is a chemical substances. By pre-treating with equimolar amounts of alkylaluminums, functional alpha-olefin 10-undecen-1-ol can be efficiently incorporated into polyethylene chains. 10-Undecen-1-ol incorporation can easily reach 15.8 mol% under the mild conditions. When compared with VCl3(THF)3 or rac-Et[Ind]2ZrCl2, these vanadium(III) complexes exhibited higher activities towards the copolymerization, and can incorporate more 10-undecen-1-ol into polymer chains under the similar conditions[3]. Direct UV photochemical functionalization of H-terminated Si(111) with bifunctional 10-undecen-1-ol was achieved with selective attachment via its vinyl end, resulting in the formation of a compact monolayer with free terminal alcohol groups. This is due to the faster radical propagation mechanism in hydrosilylation with alkene compared to the nucleophilic attack mechanism of alcohol, which is impeded by intermolecular hydrogen bonding present at room temperature[4]. The polyester channels modified with 10-undecen-1-ol exhibited a dramatically high-separation efficiency compared with the conventional fused-silica capillary tubes[5].

10-Undecen-1-ol/十一烯醇 参考文献

[1]Quinzler D, et al. Renewable resource-based poly(dodecyloate) by carbonylation polymerization. Chem Commun (Camb). 2009;(36):5400-5402.

[2]Jonas U. A, et al. Functional Beads of Polyvinylpyrrolidone: Promising Support Materials for Solid‐Phase Synthesis.

[3]Xu BC, Hu T, Wu JQ, Hu NH, Li YS. Novel vanadium(III) complexes with bidentate N,N-chelating iminopyrrolide ligands: synthesis, characterization and catalytic behaviour of ethylene polymerization and copolymerization with 10-undecen-1-ol. Dalton Trans. 2009;(41):8854‐8863

[4]Zhong YL, Bernasek SL. Direct photochemical functionalization of Si(111) with undecenol. Langmuir. 2011;27(5):1796‐1802

[5]Xu W, Uchiyama K, Shimosaka T, Hobo T. Fabrication of polyester microchannels and their applications to capillary electrophoresis. J Chromatogr A. 2001;907(1-2):279‐289

10-Undecen-1-ol/十一烯醇 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

5.87mL

1.17mL

0.59mL

29.36mL

5.87mL

2.94mL

58.72mL

11.74mL

5.87mL

10-Undecen-1-ol/十一烯醇 技术信息

CAS号112-43-6
分子式C11H22O
分子量 170.29
SMILES Code C=CCCCCCCCCCO
MDL No. MFCD00004750
别名 10-十一烯-1-醇
运输蓝冰
InChI Key GIEMHYCMBGELGY-UHFFFAOYSA-N
Pubchem ID 8185
存储条件

In solvent -20°C:3-6个月-80°C:12个月

溶解方案 请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
方案一
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