1) Anhydrous zinc bromide
烯丙基溴化镁
2) allyl alcohol
烯丙醇
1.
Study on the kinetics of allyl alcohol epoxidition to glycidol over Ti-MWW catalyst;
Ti-MWW催化烯丙醇环氧化制环氧丙醇的动力学研究
2.
Preparation of allyl alcohol by isomerization of propylene oxide over lithium phosphate catalysts;
磷酸锂催化剂上环氧丙烷异构化制烯丙醇的研究
3) allyl chloride
烯丙基氯
1.
Allylsucrose was prepared by the reaction of sucrose with allyl chloride as the etherification agent in the presence of NaOH as an activating agent.
以蔗糖为原料,NaOH为活化剂对蔗糖进行活化预处理,烯丙基氯为醚化试剂,制备了烯丙基蔗糖(AS)。
2.
Flame retardant bis(4-allyloxy-3,5-dibromophenyl)sulfone(ATBS) with high yield and high mass fraction was obtained by etherization of bis(4-hydroxy-3,5-dibromophenyl)sulfone(TBS) with allyl chloride in the presence of alkaline medium and under low pressure(gauge pressure 0.
用四溴双酚S(TBS)和烯丙基氯为原料,在NaOH水介质中,低压条件下(表压0。
3.
High yield and purity flame retardant bis-(4-allyloxy-3,5-dibromophenyl)sulfone(ATBS) was obtained by allyl-etherizing bis-(4-hydrxy-3,5-dibromophenyl)sulfone(TBS) with dropping allyl chloride in aqueous NaOH in the presence of cetyltrimethylammonium bromide(CTAB) or other surfactants.
用四溴双酚S(TBS)为原料,以滴加方式加入醚化剂烯丙基氯,在NaOH水溶液中用十六烷基三甲基溴化铵(CTAB)催化醚化法和其它表面活性剂促进醚化法合成了收率、纯度均较高的阻燃剂四溴双酚S双烯丙基醚(ATBS)。
4) allethrolone
烯丙醇酮
1.
The resolution of racemic allethrolone (4-hydroxy-3-methyl-2-(2-propenyl)-2-cyclopenten-1-one) catalyzed by lipase instead of chemical methods was investigated.
试图应用脂肪酶催化拆分法代替化学法拆分外消旋烯丙醇酮(4-羟基-3-甲基-2-(2-烯丙基)-2-环戊烯-1-酮,allethrolone)。
2.
The resolution of allethrolone.
expansumPED03脂肪酶在非水相中对外消旋烯丙醇酮(4羟基3甲基2(2烯丙基)2环戊烯1酮,allethrolone)进行酶法拆分,35℃反应36h时转化率(C)可达理论值的96%,产物的对映体过量值(eep)可达99%,显示了良好的应用潜力。
3.
The advantages and disadvantages of different methods were summarized on the chiral resolution of allethrolone.
烯丙醇酮是合成高效低毒杀虫剂烯丙菊酯的重要中间体之一,寻求一种好的拆分外消旋体烯丙醇酮的方法是极其重要的。
5) Acrylic ester
烯丙酸酯
6) Allyl group
烯丙基
1.
A novel method for preparing thermosetting modified polyphenylene ether was investigated by introducing allyl group into polyphenylene ether (PPE).
通过溴化聚苯醚和格利雅试剂反应,将不饱和基团烯丙基引入聚苯醚中实现其热固性改性,由1H-NMR和FTIR进行结构表征。
参考词条
补充资料:丙基溴
分子式:C3H7Br
分子量:123.00
CAS号:106-94-5
性质:无色易燃液体。熔点-110℃,沸点71℃,相对密度1.3537(20/4℃),折光率1.4343,折射率1.434,闪点25℃。能与醇、醚混溶,微溶于水。
制备方法:(1)由正丙醇与氢溴酸反应而得。将氢溴酸加入浓硫酸中,再加入正丙醇,加热回流0.5h。于70-75℃将生成的溴丙烷全部蒸出,然后用浓盐酸洗,再用碳酸钠中和至pH为7。用无水硫酸钠干燥,过滤,滤液蒸馏,收集69-74℃馏分,得溴丙烷。(2)由正丙醇与溴化钠反应而得。将正丙醇和水、溴化钠一起加热至回流,保持69-72℃滴加硫酸,加毕,继续回流2h。蒸馏,收集68-100℃馏出液,用碳酸钠溶液洗至中性,再蒸馏,收集68-76℃馏出液即溴丙烷。另外,在红磷存在下,正丙醇与溴反应也可制备溴丙烷。
用途:用于医药、农药、染料、香料等制造,还用作Grignard试剂的原料,药物丙硫硫胺,丙磺舒的中间体。
分子量:123.00
CAS号:106-94-5
性质:无色易燃液体。熔点-110℃,沸点71℃,相对密度1.3537(20/4℃),折光率1.4343,折射率1.434,闪点25℃。能与醇、醚混溶,微溶于水。
制备方法:(1)由正丙醇与氢溴酸反应而得。将氢溴酸加入浓硫酸中,再加入正丙醇,加热回流0.5h。于70-75℃将生成的溴丙烷全部蒸出,然后用浓盐酸洗,再用碳酸钠中和至pH为7。用无水硫酸钠干燥,过滤,滤液蒸馏,收集69-74℃馏分,得溴丙烷。(2)由正丙醇与溴化钠反应而得。将正丙醇和水、溴化钠一起加热至回流,保持69-72℃滴加硫酸,加毕,继续回流2h。蒸馏,收集68-100℃馏出液,用碳酸钠溶液洗至中性,再蒸馏,收集68-76℃馏出液即溴丙烷。另外,在红磷存在下,正丙醇与溴反应也可制备溴丙烷。
用途:用于医药、农药、染料、香料等制造,还用作Grignard试剂的原料,药物丙硫硫胺,丙磺舒的中间体。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。