苯酰胺

The graft copolymer has an optimum effect of pour point depressing for the Daqing crude oil when it was synthesized under the conditions of that the mole ratio of EVA and octadecyl maleimide was 1:20, mass fraction peroxidation benzoin formyl was 2.5%, polymerization time was 6h, and the polymerization temperature was 90℃.

以目标物的降凝幅度为评价指标，优选出适合的合成条件为：EVA与十八烷基马来酰亚胺的摩尔比为1：20，引发剂过氧化二苯甲酰的量为2.5%，聚合时间6h，聚合温度为90℃。

The reaction of benzoic acid and ethylenediamine was studied under different conditions.

在不同条件下考察了苯甲酸与乙二胺的反应，对反应产物、主要副产物及反应中间体进行了分离和鉴定，通过熔点测定、元素分析和红外光谱分析，确定了产物为2-苯基咪唑啉，主要副产物为二苯甲酰乙二胺，中间体之一为乙二胺与苯甲酸形成的双盐。

Market sales of goods is actually soluble saccharin of the sodium o-benzoyl imide salt, Shaodai colorless crystal or white crystalline powder, odorless or slight odor, known saccharin sodium.

商品市场销售实际上是可溶性糖精的钠邻苯甲酰磺酰亚胺盐，Shaodai无色结晶或白色结晶性粉末，无臭或稍有气味，已知的糖精钠。

Project Background and Conditions: The company started research new chemical products in 1998. After two years of efforts, a series of pharmaceutical intermediate sulfathiazole leave instructions, including : 3- methyl sulfathiazole leave instructions, 2- sulfathiazole leave instructions ethanoic acid, 2- acetyl sulfathiazole leave instructions, 2-thiofuran amino ethane ,2-thiofuran acetic, 3,4,5- tighter nitrobenzene have been successfully developed. 2-thiofuran amino ethane are the precursors raw materials of series antibiotic analgesic.

二、项目建设背景及条件：1998年公司开始研究开发高新精细化工产品，经过两年的努力，已成功研制出噻吩系列医药中间体，包括：3-甲基噻吩、2-噻吩乙酸、2-乙酰噻吩、2-噻吩乙胺、2-噻吩乙醇、3，4，5-三氯硝基苯等。2-噻吩乙胺系列噻吩产品使用于血小板及血栓有关的心脏血管病及消炎镇痛等如氯吡格雷、兴孢噻吩钠、兴孢西丁、噻吩洛酸等十几种新药的前体原料，是国家政策鼓励发展和有自主知识产权的项目。

Phthalimide,anthranilic acid,2methyleneglutaronitrile bromina 1bromobutane 1,2benzisothiazole3one.

邻苯二甲酰亚胺，邻氨基苯甲酸，2亚甲基戊二脯，2溴2溴甲基戊二脯，溴代正丁烷，1.2苯并异噻唑3酮。

By using 4-chloro-5-nitro phthalimide as raw material and through aminoysis, reduction, cyclization and hydrolysis, end-produce benzimidazole-5,6-diformic acid is prepared.

本发明公开了一种苯并咪唑－5，6－二甲酸的制备方法。该方法是以4－氯－5－硝基邻苯二甲酰亚胺为原料，依次经过氨解、还原、环合、水解反应过程，制得最终产品苯并咪唑－5，6－二甲酸。

Keywords acylhydrazone;sulfamic acid;N-aminophthalimide;fine chemical intermediate

酰腙； 氨基磺酸； N-氨基邻苯二甲酰亚胺；精细化工中间体

Our method featured employing the glycosyl donor with Bz as the protectivegroups and 0.05 equiv of TMSOTf as the promoter.

即：用苯甲酰基保护的三氯乙酰亚胺酯作给体，用5％当量的TMSOTf作促进剂，在室温下反应5min至15min。

Our method featured employing the glycosyl donor with Bz as the protective groups and 0.05 equiv of TMSOTF as the promoter.

即：用苯甲酰基保护的三氯乙酰亚胺酯作给体，用 5%当量的 TMSOTf 作促进剂，在室温下反应 5 min 至 15 min。

A series of imides oligomers were synthesized with the phenylethynylphthalic anhydride , nadic anhydride and cyanophthalic anhydride as endcapped agents.

我们以苯乙炔苯酐、降冰片烯二酸酐和氰基苯酐为封端剂合成了一系列的酰亚胺低聚物。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。