1) 1,2-bis(4-carboxyaldehydephenoxy)ethane
1,2-双(4-甲酰基苯氧)乙烷
1.
The target compounds were synthesized in acetic acid by condensation of the substituted 1,2,4-triazole and the intermediates 1,2-bis(2-carboxyaldehydephenoxy)ethane and 1,2-bis(4-carboxyaldehydephenoxy)ethane,which were produced from the condensation of salicyladehyde and p-hydroxybenzaldehyde with 1,2-dibromo-enthane.
以水杨醛和对羟基苯甲醛为起始原料,与1,2-二溴乙烷缩合得中间体1,2-双(2-甲酰基苯氧)乙烷和1,2-双(4-甲酰基苯氧)乙烷,再与取代的1,2,4-三唑在醋酸回流下缩合,即制得相应的目标化合物三唑席夫碱。
2) 1,1'-[1,2-ethanediylbis(oxy)]bis[3-methyl-benzen
1,2-双(3-甲基苯氧基)乙烷
3) 1-(2-Methoxyethyl)-4-(oxiranylmethoxy)benzene
3-[4-(2-甲氧乙基)苯氧基]-1,2-环氧丙烷
4) 1,2-bis(4-hydroxy-3-methoxyphenyl)ethane
1,2-二(3-甲氧基-4-羟基苯基)乙烷
5) p-Propionyltoluene
4-甲苯酰基乙烷
6) 2,5-bis(4-methoxybenzoyl)styrene
2,5-双(4-甲氧基苯甲酰氧基)苯乙烯
补充资料：[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式：C16H16ClN3O3S
分子量：365.5
CAS号：26807-65-8
性质：暂无
制备方法：暂无
用途：用于轻、中度原发性高血压。
分子量：365.5
CAS号：26807-65-8
性质：暂无
制备方法：暂无
用途：用于轻、中度原发性高血压。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条