CAS: 5453-88-3; Ethyl 1-Methyl-2-Oxocyclopentanecarboxylate
该化合物是一个有机化合物,其特性为酯功能组,其产物为环戊烷丙烯酯酸和乙醇,其特性为环戊烷环,其中含有一个酮和一个箱内酯组,其独特的化学特性有所助益;其典型的颜色无色可粉黄色液体,其香味可观,使其在口味和香味应用中可能有用;氧化物组(氯酮)的存在可增强其再活动性,允许各种化学变异,例如核脑哲学添加物;乙酰1-甲基-2环丙烯丙烯酯在有机溶剂中是可溶的,在标准条件下具有中等稳定性;其分子结构表明有机合成的潜在应用,特别是在制药或农用化学物的开发中.然而,由于许多有机化合物,在处理时应采取安全防范措施,因为如果在生产或吸入时可能会对健康造成危害.
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- 产品信息参考
;;;; - InChIKey: UIZCVGDHOSROCR-UHFFFAOYSA-N
- InChI=1/C9H14O3/c1-3-12-8(11)9(2)6-4-5-7(9)10/h3-6H2,1-2H3
- 计算化学: 氢键受体数3.0氢键供体数0.0可旋转键数2.0
相似化合物
10316-60-6 16428-99-2 55285-79-5物理性质
MSDS等安全信息
欧盟法规
C&L通报上下游产品
methyl bromide Sodium; 2-ethoxycarbonyl-cyclopent-1-enolate dimethyl sulfate methyl iodide2-methyl-adipic acid diethyl ester ethyl 3-methyl-2-ox°Cyclopentanecarboxylate (6-Methyl-1,4-dioxa-spiro[4.4]non-6-yl)-methanol N-(2-carboethoxy-2-methylcyclopentylidene)-β-phenethylamine合成工艺路线路线简述
- 合成目标产物 Ethyl1-Methyl-2-Oxocyclopentanecarboxylate 主要起始原料 Ethyl 2-Oxocyclopentanecarboxylate And Iodomethane
- (文献来源)合成步骤主要原料 Ethyl 2-Oxocyclopentanecarboxylate 和 Iodomethane
📜Alkaline Earth Salt Of/the/ Methylsulfuric Acid置于铬酸体系中,化学反应生成 1-甲基-2-氧代环戊烷-1-羧酸乙酯
参考文献:Dieckmann,Justus Liebigs Annalen Der Chemie,1901,Vol. 317,P. 104
标题:Dieckmann,Justus Liebigs Annalen Der Chemie,1901,Vol. 317,P. 104
海关参考信息
- 2905121000-正丙醇
2909110000-乙醚
2912110000-甲醛
2912120000-乙醛 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-1597650-A
优先权日:2003-09-18
标题:A kind of ether compound containing cyclopentyl group and its synthesis method and application
专利号:CN-1789234-A
优先权日:2004-12-16
标题:A kind of 2-alkoxycyclopentyl ester compound and its synthesis method and application
专利号:CN-100348571-C
优先权日:2004-12-16
标 题:A kind of 2-alkoxycyclopentyl ester compound and its synthesis method and application
专利号:CN-100338018-C
优先权日:2004-10-29
标 题 :A kind of cyclopentyl ester compound and its synthesis method and application
专利号:CN-1247508-C
优先权日:2003-09-18
标 题:A kind of ether compound containing cyclopentyl group and its synthesis method and application
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:The α-Effect In The Stereochemistry Of Kinetic Ketonization Of Enols1,2作者:Howard E. Zimmerman,Pengfei Wang |发布日期:2003.11.1
摘要:Organic Reactions. Protonation Occurring From The Less Hindered Side Of The, E.G., Enolic System Affords The Less Stable Of Two Diastereomers. However, One Apparent Discrepancy Has Been In The Synthesis Of Prostaglandins. The Present Research Deals With The Source Of This Behavior. A Curious Effect Of The Substituent At The Enolic Alpha Carbon Was Uncovered. In Certain Instances An Alpha Substituent Is
合成参考文献
摘要:Maier, M. E., Science of Synthesis, (2007) 20, 1502.
摘要:Leung, M.-k.; Luh, T.-Y., Science of Synthesis, (2007) 30, 290.
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