CAS: 41519-18-0; 2-Butenoic Acid, 2-Methyl-, 3-Methylbutyl Ester, (2E)-

该化合物是因四酸和异氨醇反应而形成的酯类化合物,由于果类,植物和少量草本芳香,通常用作香味成分.该化合物与多种香味配方具有良好的稳定性和兼容性,适合用于香水和口味应用.其清晰,无色和淡黄色的液体形式确保了处理和混合的便利.Isoamyl Tiglate因其能够增强顶部和中层音质的构成能力而备受重视,有助于形成新鲜,绿色的特性.其低波动性和中度的坚固度为各种产品矩阵提供了平衡的性能.

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上下游产品

Tiglic acid i-Amyl alcohol

合成工艺路线路线简述

  • 合成目标产物 Isoamyl Tiglate 主要起始原料 Tiglic Acid And 3-Methyl-1-Butanol
  • (文献来源)合成步骤主要原料 Tiglic Acid 和 3-Methyl-1-Butanol
📜惕格酸,异戊醇置于吡啶,4-二甲氨基吡啶体系中,用 二氯甲烷 作为反应溶剂,化学反应 2.5H,以78%的收率获得产物惕各酸异戊酯
参考文献:Nematicidal Activity Of Natural Ester Compounds And Their Analogues Against Pine Wood Nematode,Bursaphelenchus Xylophilus
标题:Nematicidal Activity Of Natural Ester Compounds And Their Analogues Against Pine Wood Nematode,Bursaphelenchus Xylophilus
摘要:In This Study,We Evaluated The Nematicidal Activity Of Natural Ester Compounds Against The Pine Wood Nematode,Bursaphelenchus Xylophilus,To Identify Candidates For The Development Of Novel,Safe Nematicides. We Also Tested The Nematicidal Activity Of Synthesized Analogues Of These Ester Compounds To Determine The Structure-Activity Relationship. Among 28 Ester Compounds Tested,Isobutyl 2-Methylbutanoate,3-Methylbutyl 2-Methylbutanoate,3-Methylbutyl Tiglate,3-Methyl-2-Butenyl 2-Methylbutanoate,And Pentyl 2-Methylbutanoate Showed Strong Nematicidal Activity Against The Pine Wood Nematode At A 1 Mg/ml Concentration. The Other Ester Compounds Showed Weak Nematicidal Activity. The Lc50 Values Of 3-Methylbutyl Tiglate,Isobutyl 2-Methylbutanoate,3-Methylbutyl 2-Methylbutanoate,3-Methyl-2-Butenyl 2-Methylbutanoate,And Pentyl 2-Methylbutanoate Were 0.0218,0.0284,0.0326,0.0402,And 0.0480 Mg/ml,Respectively. The Ester Compounds Described Herein Merit Further Study As Potential Nematicides For Pine Wood Nematode Control.
DOI:10.1021/jf503631E

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✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1186/1471-2105-14-s19-s6
摘要:Strauch M, Müthing C, Broeg MP, Szyszka P, Münch D, Laudes T, Deussen O, Galizia CG, Merhof D. The looks of an odour - Visualising neural odour response patterns in real time. BMC Bioinformatics. 2013 Nov 12;14(Suppl 19):s6. doi: 10.1186/1471-2105-14-s19-s6.
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