CAS: 20815-29-6; 4-Ethyl-3-Methylpyridine

该化合物是属于含有环内氮原子的丙烯的有机化合物,是含有环内氮原子的芳香异环化合物;这种特殊化合物具有四方的乙基组和三方的丙烯环的三方的甲基组;一种无色的黄色液体,具有典型的气味,在水溶液中溶解有限的情况下,可溶于有机溶剂中;乙基和甲基替代品的存在影响其物理和化学特性,如沸点和再活动. 4-乙基-3-甲基丙烯可参与典型的,有虫性衍生物的各种化学反应,包括生物电子替代和核分裂反应;它经常用于有机合成,并可作为生产药品,农用化学品和其他精密化学品的中间体.安全数据表明,应当谨慎处理,因为它可能对皮肤和眼睛产生刺激,如果吸入或吸入,则会构成健康风险.

结构式图片

相似化合物

98009-88-2 529-21-5 3478-72-6

上下游产品

CAS号96-22-0 3-戊酮 | CAS号290-38-0 [1,2,4]三嗪 | CAS号56176-59-1 1-pent-2-en-3-y... | CAS号108-99-6 3-甲基吡啶 | CAS号64-17-5 乙醇 | CAS号108-24-7 乙酸酐 | CAS号2386-64-3 乙基氯化镁

合成工艺路线路线简述

  • 合成目标产物 3-Methyl-4-Ethyl Pyridine 主要起始原料 3-Pentanone And 1,2,4-Triazine
  • (文献来源)合成步骤主要原料 3-Pentanone 和 1,2,4-Triazine
📜1-(2,5-Dimethyl-Pyrrol-1-yl)-4-Ethyl-3-Methyl-1,4-Dihydro-Pyridine置于偶氮二异丁腈体系中,用 四氢呋喃 用作溶剂,化学反应 24.0H,以77%的收率获得4-乙基-3-甲基吡啶
参考文献:Katritzky,Alan R.; Beltrami,Hector; Sammes,Michael P.,Journal Of Chemical Research,Miniprint,1981,# 5,P. 1684-1696
标题:Katritzky,Alan R.; Beltrami,Hector; Sammes,Michael P.,Journal Of Chemical Research,Miniprint,1981,# 5,P. 1684-1696

海关参考信息

专利信息


专利号:US-3829428-A
优先权日:1972-09-01
标题 :Process for the catalytic vapor-phase synthesis of alkylpyridines
发明人:HARGIS C
权利人:EASTMAN KODAK CO
摘要:PROCESS FOR THE VAPOR-PHASE PRODUCTION OF 2- AND 4PICOLINE WHICH COMPRISES CONTACTING A MIXTURE OF AMMONIA AND ACETALDEHYDE IN THE VAPOR-PHASE AT AN ELEVATED TEMPERATURE IN THE PRESENCE OF A CATALYST OF SILICA-ALUMINA AND A CO-CATALYST SELECTED FROM LITHIUM PHOSPHATE, NIOBIUM PENTOXIDE, TANTIALUM PENTIOXIDE, BISMUTH TRIOXIDE, ANTIMONY (IV) OXIDE, OR A MIXTURE OF ANTIMONY (IV) OXIDE AND POTASSIUM OXIDE.

专利号:US-4042602-A
优先权日:1976-11-04
标题 :Synthesis of dideoxyzearalane and related compounds
发明人:ROBERTSON DONALD EDWIN; URRY WILBERT HERBERT; KAVKA FRANK
权利人:IMC CHEMICAL GROUP
摘要:A method is disclosed for preparing dideoxyzearalane and related compounds which comprises reacting a hexahydrozearalin with an organic sulfonyl chloride to form a sulfonate ester derivative; recovering the sulfonate ester derivative; and catalytically dehydrosulfonyloxylating and aromatizing the sulfonate ester derivative to form the desired product.

专利号:US-3631021-A
优先权日:1969-04-15
标题 :7-halo lincomycin carbonate esters
发明人:SINKULA ANTHONY A
权利人:UPJOHN CO
摘要:THIS INVENTION RELATES TO NOVEL 3-MONO(ALKYL CARBONATE) AND 2,3-BIS(ALKYL CARBONATE) ESTERS OF 7-HALOGENATED LINCOMYCIN COMPOUNDS OF THE FORMULA 2-(R-S-),3-(R4-O-),4-(R3-O-),5-(HO-),6-((1-R2,4-R1- PYRROLIDIN-2-YL)-CO-NH-CH(-CH(-X)-CH3)-)TETRAHYDROPYRAN WHEREIN R IS ALKYL OF FROM 1 THROUGH 6 CARBON ATOMS; R1 IS ALKYL OF FROM 1 THROUGH 8 CARBON ATOMS, CYCLOALKYL OF FROM 3 THROUGH 8 CARBON ATOMS, OR ARALKYL OF UP TO 12 CARBON ATOMS; R2 IS HYDROGEN OR ALKYL OF FROM 1 THROUGH 8 CARBON ATOMS; X IS CHLORINE, BROMINE OR IODINE; R3 IS CNH(2N+1)-OOC- WHEREIN N IS AN INTEGER FROM 1 THROUGH 20 AND R4 IS R3 OR HYDROGEN; THEIR ACID ADDITION SALTS; AND NOVEL SYNTHESIS PROCESSES. THESE ALKYL CARBONATE ESTERS OF LINCOMYCIN COMPOUNDS HAVE ANTIBIOTIC ACTIVITY. FOR EXAMPLE, THE 3-MONO(ALKYL CARBONATE) ESTERS CAN BE USED TO INHIBIT THE GROWTH OF STAPHYLOCOCCUS AUREUS, STREPTOCOCCUS HEMOLYTICUS AND STREPTOCOCCUS FAECALIS ON MEDIAL AND DENTAL EQUIPMENT CONTAMINATED WITH THESE BACTERIA. THE 2,3-BIS(HEXLY CARBONATE) ESTER OF 7-DEOXY-7(S)-CHLOROLINCOMYCIN IS ADVANTAGEOUS FOR ORAL ADMINISTRATION AS AN ANTIBIOTIC IN THAT IT LACKS THE BITTER TASTE OF THE UNESTERIFIED COMPOUND.

专利号:US-4222962-A
优先权日:1978-12-11
标 题:Process for preparing a substituted diphenoxybenzene
发明人:PELLEGRINI JR JOHN P
权利人:GULF RESEARCH DEVELOPMENT CO
摘要:A diaminophenoxy or a dinitrophenoxybenzene is prepared in good yield from dibromobenzene and an alkali metal salt of meta-aminophenol or meta-nitrophenol under Ullmann ether synthesis conditions at low temperatures of 115° C. to 150° C.

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1055/s-2006-926236
摘要:Kiselyov A. A Domino Cyclization Reaction of Iminium Salts: A Convenient Route to Hexahydrobenzo[b]phenanthrolines. Synlett. 2006 Feb 06;2006(03):0391–4. doi: 10.1055/s-2006-926236.
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