CAS: 5535-52-4; P-Tolylvinylsulphone

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2-(p-tolylsulfonyl)ethanol p-tolyl vinyl sulfide 2-chloroethyl-p-toluenesulfonate triethylamine1-[2-(toluene-4-sulfonyl)-ethyl]-piperidine 1,2-bis(p-tolylsulfonyl)ethane 3-nitro-1,5-bis-(toluene-4-sulfonyl)-pentane 3-[(4-methylbenzene)sulfonyl]propanenitrile

合成工艺路线路线简述

  • 合成目标产物 P-Tolyl Vinyl Sulphone 主要起始原料 Benzenepropanoic Acid, 2-[(4-Methylphenyl)Sulfonyl]Ethyl Ester
  • (文献来源)合成步骤主要原料 Benzenepropanoic Acid, 2-[(4-Methylphenyl)Sulfonyl]Ethyl Ester
📜2-氯乙基对甲苯基砜置于三乙胺体系中,化学反应 24.0H,以80%的收率获得产物对甲苯基乙烯基砜
参考文献:Alonso,Diego A.; Arques,Antonio; Najera,Carmen,Anales De Quimica,1995,Vol. 91,# 5-6,P. 449-452
标题:Alonso,Diego A.; Arques,Antonio; Najera,Carmen,Anales De Quimica,1995,Vol. 91,# 5-6,P. 449-452

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专利信息


专利号:WO-2007064291-A1
优先权日:2005-11-30
标 题:Method and compounds for rna synthesis
发明人:CHATTOPADHYAYA JYOTI
权利人:CHATTOPADHYAYA JYOTI
摘要:The 2-(4-tolylsulfonyl)ethoxymethyl (TEM) as a new 2'-OH protecting group is reported for the RNA synthesis on the solid support using the phosphoramidite chemistry. The usefulness of the 2'-0-TEM group is exemplified by the synthesis of 12 different oligo-RNAs of various sizes (14-38nt long). The stepwise coupling yield varied from 97 - 99 % with an optimized coupling time of 120s. Synthesis of all four pure phosphoramidite building blocks are also described. Two new reliable parameters, δc2' - δc3s and δn2' - δH3' have been suggested for the characterization of isomeric 2'-0-TEM and 3'-0-TEM as well as other isomeric mono 273 '-protected ribonucleoside derivatives. The most striking feature of this strategy is that the crude RNA prepared using our 2'-0-TEM strategy is sufficiently pure (>90 %) for molecular biology research without any additional purification step, thereby making oligo-RNAs easily available at a relatively low cost, saving both time and lab resources.

专利号:CN-105566235-A
优先权日:2016-03-03
标题:Method for step-by-step synthesis of NH-1,2,3-triazoles catalyzed by aluminum salts

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合成参考文献


摘要:Snaith, J. S., Science of Synthesis Knowledge Updates, (2011) 2, 214.
摘要:Duschmalé, J.; Arakawa, Y.; Wennemers, H., Science of Synthesis: Asymmetric Organocatalysis, (2012) 2, 741.
摘要:Paterson, A. J.; Beke-Somfai, T.; Kann, N., Science of Synthesis, (2021) , 293.
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