1) 2-hydroxy-meta-toluic acid
２-羟基间甲苯酸
2) citramalic acid
２-甲基-２-羟基丁二酸
3) 2-anilinobenzoic acid
２-苯胺基苯甲酸
4) m-hydroxybenzoic acid
间羟基苯甲酸
1.
Seven methods of synthesis of m-hydroxybenzoic acid(1) were reviewed and their advantages and disadvantages were also discussed in this paper.
介绍了七种合成间羟基苯甲酸(1)的方法,并对这些方法的优缺点进行了讨论。
5) m-Hydroxybenzoic Acid (mHBA)
间羟基苯甲酸(MHBA)
6) m hydroxybenzoic acid
间羟基苯甲酸
1.
The separation behavior of o hydroxybenzoic acid, m hydroxybenzoic acid and p hydroxybenzoic acid in high performance capillary zone electrophoresis was investigated using cetyltrimethylammonium bromide(CTAB) as reversed reagent for electroosmotic flow The effects of pH of buffer solution and volume fraction of methanol on the separation, peak shape and elution order were studie
采用十六烷基三甲基溴化铵 (CTAB)为电渗流改性剂 ,考察了邻羟基苯甲酸、间羟基苯甲酸和对羟基苯甲酸在高效毛细管区带电泳模式下的分离行为 ,研究了缓冲液的pH和添加剂甲醇的用量对这 3种同分异构体的分离、峰形和出峰顺序的影响 ,并据此优化了这 3种异构体的分离条件。
2.
A method for the simultaneous determination of m hydroxybenzoic acid and p hydroxybenzoic acid is proposed.
利用导数分光光度法同时测定了间羟基苯甲酸和对羟基苯甲酸。
3.
The synthesis of m hydroxybenzoic acid was made from benzoic acid by sulfonation followed by reaction with alkali metal hydroxide.
以苯甲酸为原料经磺化及碱熔两步反应合成间羟基苯甲酸，研究了反应的主要影响因素。
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