苯甲酰氯；[有化]氯化苯甲酰

benzyl chloride───氯化苄；[有化]苄基氯

benzal chloride───[有化]苄叉二氯；二氯甲基苯

benzyl chlorides───氯化苄；[有化]苄基氯

benzyl dichloride───二氯化苄

benzal chlorides───[有化]苄叉二氯；二氯甲基苯

benzotrichloride───n.三氯甲苯；[有化]苄川三氯

benzoyl peroxide───过氧化苯甲酰

benzoyl chloride by acids lation hydrogenation cyclization with an overall yield of8.05%.───甲酰氯为原料，经酰化，还原，环合等反应合成左旋西替利嗪盐酸盐，反应总收率为8。05%。

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation, hydrogenation, cyclization with an overall yield of 8.05 %.───以苯甲酰氯为原料,经酰化, 还原, 环合等反应合成左旋西替利嗪盐酸盐,反应总收率为8.05%.

A new photoinitiator, 4-phenoxy benzophenone (PBZP), was synthesized and characterized using diphenyl ether and benzoyl chloride as raw material.───以二苯醚与苯甲酰氯为原料，合成了一种新型的激光光敏刺——4 -苯氧基二苯甲酮(PBZP)。

Preparation methods of benzoyl cyanate were reviewed. The optimal conditions of synthesis of benzoyl cyanate from benzoyl amine and oxalyl chloride were investigated.───综述了苯甲酰异氰酸酯的合成路线，并探讨了利用苯甲酰胺与草酰氯制备苯甲酰异氰酸酯的最佳反应条件。

A new photoinitiator, 4-phenoxy benzophenone (PBZP), was synthesized and characterized using diphenyl ether and benzoyl chloride as raw material.

Benzoyl chloride and ethyl acetoacetate react and hydrolyze in the presence of a catalyst to synthesize ethyl benzoylacltete, yielding 60%, with a purity of more than 98%.

After hydrazinolysis, hydrazide resin (3 ) reacted further with substituted benzoyl chloride obtaining hydrazide resin (4).

Methods: It takes Benzoyl chloride and Ethyl acetoacetate as its initial raw materials. It is made by two steps of acylation and hydrolysis.

Benzoyl chloride was synthesized by the reaction of benzoic acid with SOCl2 and reacted with resorcinol to give 2,4-dihydroxy benzophenone, the yield was 79.4%.

The reaction of benzotrichloride and chloroacetic acid to form chloroacetyl chloride and benzoyl chloride in the presence of catalyst was studied.

A low-cost three-dimensional large pore HY zeolite was used in the liquid phase benzoylation of various aromatics with benzoyl chloride instead of classical homogeneous catalysts.

Levocetirizine Dihydrochloride was prepared from benzoyl chloride by acidylation, hydrogenation, cyclization with an overall yield of 8.05 %.