1) methoxymerphalane
甲氧芳芥
2) mechlorethaminoxyde
甲氧氮芥
3) aryl nitrogen mustard
芳香氮芥
1.
Synthesis and Biological Activity of Aryl Nitrogen Mustard Derivatives;
芳香氮芥衍生物的合成及生理活性研究
2.
Six aryl nitrogen mustard derivatives were designed and synthesized with N,N-di(2-chloroethyl)-1,4-phenylene diamine(4) as the pharmacophore,terpineols and linear saturated alcohols as the carrier,and carbamate as the linker.
以芳香氮芥N,N-二(2-氯乙基)-1,4-苯二胺为药效基团,不同链长的萜醇和饱和醇为载体,通过氨基甲酸酯的联接方式,设计合成了6个芳香氮芥衍生物,收率在66%~90%之间,所有目标化合物的结构均经元素分析、1HNMR、13C NMR和MS测试技术确证。
4) betamerphalan
异芳芥
5) methane dehydroaromatization
甲烷无氧芳构化
1.
In this paper, REMPI-TOFMS is applied to investigate the methane dehydroaromatization reaction, which is the earlier stage work of " the application of combinatorial chemistry in material filed".
本论文采用共振增强多光子电离耦合飞行时间质谱技术考察了甲烷无氧芳构化反应过程，是“组合化学在材料领域的应用”课题研究的前期工作。
2.
The durability of methane dehydroaromatization(MDA) has been improved by its combination with methane steam reforming(MSR).
甲烷无氧芳构化(MDA)和甲烷水蒸气重整(MSR)的耦合反应可以大幅度提高甲烷无氧芳构化反应的稳定性。
6) 2-aroxymethyloxirane derivative
2-芳氧甲基环氧烷
1.
A series of novel 3-arylmethyl-5-aroxymethylbutyrolactone derivatives were synthesized by the reaction of 2-aroxymethyloxirane derivatives with sodium diethyl α-arylmethylmalonates in yields of 13%～ 81%.
通过2-芳氧甲基环氧烷与α-芳甲基丙二酸二乙酯在乙醇钠条件下反应,合成了8个新型3-芳甲基-5-芳氧甲基丁内酯,收率为13%～81%。
补充资料：甲氧芳芥
分子式：
CAS号：
性质：又称甲氧基溶肉瘤素。白色或类白色片状结晶性粉末，熔点167～171℃(分解)。几乎不溶于水，微溶于甲醇、乙醇，易溶于稀HCl或NaOH。由间甲氧基苯胺为原料制得。为抗肿瘤药，对慢性粒细胞白血病疗效较好，对何杰金病、淋巴肉瘤、乳腺癌等亦有一定疗效。制剂有片剂、胶囊剂。
CAS号：
性质：又称甲氧基溶肉瘤素。白色或类白色片状结晶性粉末，熔点167～171℃(分解)。几乎不溶于水，微溶于甲醇、乙醇，易溶于稀HCl或NaOH。由间甲氧基苯胺为原料制得。为抗肿瘤药，对慢性粒细胞白血病疗效较好，对何杰金病、淋巴肉瘤、乳腺癌等亦有一定疗效。制剂有片剂、胶囊剂。
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