1) 9,10-Dibromoanthracene
二溴并三苯
2) ms-Dibromoanthracene
二溴并三苯
3) dibrom,naled
二溴
4) o-dibromobenzene
邻二溴苯
1.
The solid-liquid equilibrium data for the ternary mixture of o-dibromobenzene + m-dibromobenzene + p-dibromobenzene were determined by differential scanning calorimetry (DSC).
采用差示扫描量热法,通过对一系列“拟二元”物系固液平衡数据的测定,得到了邻二溴苯、间二溴苯和对二溴苯三元物系的固液平衡数据。
2.
Solid-liquid equilibrium data for three binary mixtures of o-dibromobenzene + m-dibromobenzene, p-dibromobenzene + m-dibromobenzene, and p-dibromobenzene + o-dibromobenzene were determined by differential scanning calorimetry and their corresponding eutectic type phase diagrams were presented.
采用差示扫描量热法测定了邻二溴苯与间二溴苯、对二溴苯与间二溴苯和对二溴苯与邻二溴苯的3个二元固液平衡数据,同时绘制出相应的简单低共熔型二元相图。
5) m-dibromobenzene
间二溴苯
1.
The solid-liquid equilibrium data for the ternary mixture of o-dibromobenzene + m-dibromobenzene + p-dibromobenzene were determined by differential scanning calorimetry (DSC).
采用差示扫描量热法,通过对一系列“拟二元”物系固液平衡数据的测定,得到了邻二溴苯、间二溴苯和对二溴苯三元物系的固液平衡数据。
2.
Solid-liquid equilibrium data for three binary mixtures of o-dibromobenzene + m-dibromobenzene, p-dibromobenzene + m-dibromobenzene, and p-dibromobenzene + o-dibromobenzene were determined by differential scanning calorimetry and their corresponding eutectic type phase diagrams were presented.
采用差示扫描量热法测定了邻二溴苯与间二溴苯、对二溴苯与间二溴苯和对二溴苯与邻二溴苯的3个二元固液平衡数据,同时绘制出相应的简单低共熔型二元相图。
6) p-dibromobenzene
对二溴苯
1.
The solid-liquid equilibrium data for the ternary mixture of o-dibromobenzene + m-dibromobenzene + p-dibromobenzene were determined by differential scanning calorimetry (DSC).
采用差示扫描量热法,通过对一系列“拟二元”物系固液平衡数据的测定,得到了邻二溴苯、间二溴苯和对二溴苯三元物系的固液平衡数据。
2.
1,4-Diethynylbenzene and 1,4-diethynyl-2,5-bis-nonyloxy-benzene were prepared from p-dibromobenzene derivatives and 2-methyl-but-3-yn-2-ol by two steps of Sonogashira coupling reaction and removal of acetone in an alkaline medium.
以对二溴苯衍生物和甲基丁炔醇为原料,通过Sonogashira钯催化偶联反应得到的产物,在碱性条件下脱丙酮获得1,4-二乙炔基苯和标题化合物。
3.
The effects of p-dibromobenzene and naphthalene on the reaction were studied.
以甲基氢二氯硅烷为单体,利用超声波条件下Wurtz聚合的方法,合成了可溶性聚硅烷,研究了对二溴苯和萘对反应的影响,并用红外光谱(IR)、凝胶渗透色谱(GPC)、X射线衍射(XRD)对产物进行了表征。
参考词条
补充资料：二溴并三苯
分子式：C14H8Br2
分子量：336.0252
CAS号：523-27-3
性质：黄色针状结晶，熔点226℃。能升华，氧化后生成蒽醌。溶于热苯和热甲苯，微溶于醇、醚和冷苯，不溶于水。
制备方法：由蒽溴化而得。溴化反应在室温进行，以四氯化碳作溶剂。采用80-85%蒽为原料，加溴反应半小时，产率83-88%。
用途：有机合成中间体。
分子量：336.0252
CAS号：523-27-3
性质：黄色针状结晶，熔点226℃。能升华，氧化后生成蒽醌。溶于热苯和热甲苯，微溶于醇、醚和冷苯，不溶于水。
制备方法：由蒽溴化而得。溴化反应在室温进行，以四氯化碳作溶剂。采用80-85%蒽为原料，加溴反应半小时，产率83-88%。
用途：有机合成中间体。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。