溴代辛烷,Capryl bromide,在线英语词典,英文翻译,专业英语

1) Capryl bromide

溴代辛烷

2) Caprylic bromide

溴代辛烷

3) 1-Bromooctane

溴代辛烷

4) bromination

溴代

Study on synthesis bromination derivatives of polyethylene glycol monomethyl ether;

聚乙二醇单甲醚溴代衍生物的合成研究

Comparing to different reaction methods, the method starting from 1,3-dimethyladamantane was certified with the memantine hydrochloride synthesized by bromination ,acetimidolation, hydrolysis and acidation.

通过比较不同的反应路线,确定了以1,3-二甲基金刚烷为原料,经溴代、乙酰氨基化、水解反应最后经酸化得到盐酸美金刚胺。

Bromacil was synthesized using 2-bromobutane and urea as the starting materials in three steps including condensation,cyclization and bromination with total yield of 61%.

以2-溴丁烷和尿素作为起始原料,经缩合、环化、溴代三步反应得到除草定,总收率为61%。

5) bromization

溴代

The Study on Bromization of Benzene on the Platinum Electrode By Confocal Microprobe Raman Spectroscopy;

苯在铂电极上溴代反应的共焦显微拉曼光谱研究

6) aryl bromide

溴代芳烃

Suzuki cross-coupling reactions between aryl bromides and phenylboronic acids were studied over a hydroxyapatite-supported Mn catalyst(MnHAP) for the first time.

对于不同取代基取代的溴代芳烃或苯硼酸,可以得到中等产率(18%~46%)的偶联产物。

The palladium catalyst supported on fluoride pillared layered double hydroxide(LDH-F) was prepared by the incipient wetness method,and it was used to catalyze the Heck and Suzuki coupling reactions of aryl bromides.

以氟离子插层的水滑石LDH-F为载体,用逐滴浸渍法制备了新型Pd/LDH-F催化剂,并用其催化溴代芳烃的Heck和Suzuki偶联反应。

参考词条

α-溴代萘溴代海因溴代烷烃溴代乙醚 α溴代 2-溴代萘溴代烃溴代法 1-溴代萘溴代产物二溴代烷溴代己烷介孔材料MCM-41 NoC通讯结构

补充资料：溴代辛烷

分子式：C8H17Br
分子量：193.14
CAS号：111-83-1

性质：无色液体。熔点-55℃，沸点198-200℃，相对密度1.1122(20/4℃)，折射率1.4503，闪点78℃。能与乙醇、乙醚混溶，不溶于水。

制备方法：由辛醇与氢溴酸反应而得。用硫酸将溴化钠完全溶解后，加入正辛醇，加热回流7-8h，冷后用水稀释，分出有机相，依次用水、浓硫酸，水、10%碳酸钠溶液洗涤，用无水硫酸钠干燥。蒸馏196-200℃，或91-93℃（2.93kPa）馏分，即为成品。产率90%以上。

用途：用于有机合成。菌毒清的中间体。

说明：补充资料仅用于学习参考，请勿用于其它任何用途。

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1) Capryl bromide 溴代辛烷 2) Caprylic bromide 溴代辛烷 3) 1-Bromooctane 溴代辛烷 4) bromination 溴代 1. Study on synthesis bromination derivatives of polyethylene glycol monomethyl ether; 聚乙二醇单甲醚溴代衍生物的合成研究 2. Comparing to different reaction methods, the method starting from 1,3-dimethyladamantane was certified with the memantine hydrochloride synthesized by bromination ,acetimidolation, hydrolysis and acidation. 通过比较不同的反应路线,确定了以1,3-二甲基金刚烷为原料,经溴代、乙酰氨基化、水解反应最后经酸化得到盐酸美金刚胺。 3. Bromacil was synthesized using 2-bromobutane and urea as the starting materials in three steps including condensation,cyclization and bromination with total yield of 61%. 以2-溴丁烷和尿素作为起始原料,经缩合、环化、溴代三步反应得到除草定,总收率为61%。 5) bromization 溴代 1. The Study on Bromization of Benzene on the Platinum Electrode By Confocal Microprobe Raman Spectroscopy; 苯在铂电极上溴代反应的共焦显微拉曼光谱研究 6) aryl bromide 溴代芳烃 1. Suzuki cross-coupling reactions between aryl bromides and phenylboronic acids were studied over a hydroxyapatite-supported Mn catalyst(MnHAP) for the first time. 对于不同取代基取代的溴代芳烃或苯硼酸,可以得到中等产率(18%~46%)的偶联产物。 2. The palladium catalyst supported on fluoride pillared layered double hydroxide(LDH-F) was prepared by the incipient wetness method,and it was used to catalyze the Heck and Suzuki coupling reactions of aryl bromides. 以氟离子插层的水滑石LDH-F为载体,用逐滴浸渍法制备了新型Pd/LDH-F催化剂,并用其催化溴代芳烃的Heck和Suzuki偶联反应。参考词条 α-溴代萘溴代海因溴代烷烃溴代乙醚 α溴代 2-溴代萘溴代烃溴代法 1-溴代萘溴代产物二溴代烷溴代己烷介孔材料MCM-41 NoC通讯结构补充资料：溴代辛烷分子式：C8H17Br 分子量：193.14 CAS号：111-83-1 性质：无色液体。熔点-55℃，沸点198-200℃，相对密度1.1122(20/4℃)，折射率1.4503，闪点78℃。能与乙醇、乙醚混溶，不溶于水。制备方法：由辛醇与氢溴酸反应而得。用硫酸将溴化钠完全溶解后，加入正辛醇，加热回流7-8h，冷后用水稀释，分出有机相，依次用水、浓硫酸，水、10%碳酸钠溶液洗涤，用无水硫酸钠干燥。蒸馏196-200℃，或91-93℃（2.93kPa）馏分，即为成品。产率90%以上。用途：用于有机合成。菌毒清的中间体。说明：补充资料仅用于学习参考，请勿用于其它任何用途。
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