CAS: 21190-93-2; 2-Acetyl-6-Methoxypyridine

该化合物是一种有机化合物,其特点是其环结构,代之以甲氧基组和乙酮功能组,该化合物一般呈现黄色至浅棕色外观,在乙醇和二氯甲烷等有机溶剂中可溶解,但由于其疏水特性,在水中溶解性有限;甲氧基组的存在增强了其电子施食特性,可影响其在各种化学环境中的再活动与互动;作为丙烯衍生物,该化合物可能展示生物活动,使其对制药研究感兴趣;该化合物的分子结构允许有机合成的潜在应用,特别是在发展农业化学品或药品方面;应当参考安全数据,以便处理和储存,如任何化学物质,确保采取适当的预防措施.

结构式图片

相似化合物

54221-96-4 2227723-77-3 925417-04-5

物理性质

MSDS等安全信息

欧盟法规

ECHA物质C&L通报

上下游产品

CAS号1628-89-3 2-甲氧基吡啶 | CAS号75-36-5 乙酰氯 | CAS号107465-29-2 7-methoxy-3-met... | CAS号107465-23-6 3-methyl-7-brom... | CAS号107465-22-5 (3-methyl-[1,2,...

合成工艺路线路线简述

  • 合成目标产物 2-Acetyl-6-Methoxypyridine 97 主要起始原料 2-Methoxypyridine And Acetyl Chloride
  • (文献来源)合成步骤主要原料 2-Methoxypyridine 和 Acetyl Chloride
📜7-Bromo-3-Methyl-[1,2,3]Triazolo[1,5-A]Pyridine置于selenium(Iv) Oxide体系中,用 甲醇,氯苯 用作溶剂,化学反应 20.0H,反应生成2-乙酰基-6-甲氧基吡啶
参考文献:溴三唑并吡啶上的亲核取代-通往2,6-二取代吡啶和1,3-二取代异喹啉的改进途径
标题:溴三唑并吡啶上的亲核取代-通往2,6-二取代吡啶和1,3-二取代异喹啉的改进途径
摘要:描述了2,6-二取代的吡啶和1,3-二取代的异喹啉的区域特异性合成.
Doi:10.1016/s0040-4039(00)84845-5

海关参考信息

专利信息


专利号:US-6271379-B1
优先权日:2000-03-08
标题:Intermediates useful for the synthesis of huperzine A
发明人：TUECKMANTEL WERNER; KOZIKOWSKI ALAN P
权利人:UNIV GEORGETOWN
摘要:Intermediates useful for the synthesis of huperzine A represented by the structures below, n and methods for their synthesis, wherein: n R 1 is lower alkyl, benzyl, or substituted benzyl; n X is a suitable leaving group; n Y is an electron withdrawing group that can subsequently be converted into an amino group; n one broken line is present as a carbon—carbon bond and the other broken line is absent, where the broken line forms an unconjugated carbon—carbon double bond, which double bond may be endocyclic whereby n is 3 or the double bond may be exocyclic whereby n is 2.

专利号:US-2023002426-A1
优先权日:2019-11-15
标题 :Chiral synthesis of a tertiary alcohol

专利号:WO-2021097139-A1
优先权日:2019-11-15
标 题 :Chiral synthesis of a tertiary alcohol

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主要参考文献

参考标题:Manganese(I)-Catalyzed Transfer Hydrogenation And Acceptorless Dehydrogenative Condensation: Promotional Influence Of The Uncoordinated N-Heterocycle
作者:Chong Zhang,Bowen Hu,Dafa Chen,Haiping Xia |发布日期:2019.8.26
摘要:Showed The Highest Activity. The Reactions Proceeded Well With 0.5 Mol % Of Catalyst Loading And 20 Mol % Of T-Buok At 85 °C For 24 H. Furthermore, 3 Was Also Used As A Catalyst For The Synthesis Of Primary Alcohols Via Transfer Hydrogenation Of Aldehydes And The Synthesis Of 1,2-Disubstituted Benzimidazoles And Quinolines Via Acceptorless Dehydrogenative Condensations.

合成参考文献

参考DOI号:10.1016/j.tetlet.2013.04.075
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