CAS: 40137-29-9; 4-Chloro-2-Methylbenzaldehyde

该化合物是替代苯甲醚衍生物的替代物,分别在4个和2个位置使用氯和甲基功能组分,该芳香甲醚是有机合成的多种中间体,特别是在生产药品,农用化学品和特殊化学品方面.其反应性甲醛组可产生凝聚,氧化和减少反应,而氯和甲基替代组则可加强其在再生选择性变异方面的效用.该化合物在标准条件下表现出适度稳定性,通常作为晶体固处理.其结构特征对在药用化学和材料科学应用中构建复杂的分子框架很有价值.

结构式图片

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4-dichloromethyl-4-methyl-2,5-cyclohexadienone formaldoxime 4-chloro-2-methylbenzeneamine 4-chloro-1,2-dimethylbenzene 3-(4-chloro-2-methyl-phenyl)-glutaric acid benzamineN-(4-chloro-2-methylphenyl)methylenebenzamine 4-chloro-2-methylbenzaldehyde ethylene acetal 2-methyl-4-chlorobenzyl alcohol

合成工艺路线路线简述

    4-二氯甲基-4-甲基-2,5-环己烷二酮置于五氯化磷体系中,化学反应生成 4-氯-2-甲基苯甲醛
    参考文献:Auwers; Keil,Chemische Berichte,1905,Vol. 38,P. 1693
    标题:Auwers; Keil,Chemische Berichte,1905,Vol. 38,P. 1693

    海关参考信息

    专利信息


    专利号:US-4710513-A
    优先权日:1979-08-17
    标 题:Substituted pyranone inhibitors of cholesterol synthesis
    发明人:WILLARD ALVIN K; NOVELLO FREDERICK C; HOFFMAN WILLIAM F; CRAGOE JR EDWARD J
    权利人:MERCK & CO INC
    摘要:6-Phenyl-, phenylalkyl- and phenylethenyl-4-hydroxytetrahydropyran-2-ones in the 4(R)-trans stereoisomeric forms are potent inhibitors of cholesterol synthesis by virtue of their ability to inhibit the enzyme, 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

    专利号:US-4459422-A
    优先权日:1979-08-17
    标 题:Substituted pyranone inhibitors of cholesterol synthesis
    发明人:WILLARD ALVIN K; NOVELLO FREDERICK C; HOFFMAN WILLIAM F; CRAGOE JR EDWARD J
    权利人:MERCK & CO INC
    摘要:6-Phenyl-, phenylalkyl- and phenylethenyl-4-hydroxytetrahydropyran-2-ones in the 4(R)-trans stereoisomeric forms are potent inhibitors of cholesterol synthesis by virtue of their ability to inhibit the enzyme, 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

    专利号:US-4375475-A
    优先权日:1979-08-17
    标 题 :Substituted pyranone inhibitors of cholesterol synthesis
    发明人:WILLARD ALVIN K; NOVELLO FREDERICK C; HOFFMAN WILLIAM F; CRAGOE JR EDWARD J
    权利人:MERCK & CO INC
    摘要:6-Phenyl-, phenylalkyl- and phenylethenyl-4-hydroxytetrahydropyran-2-ones in the 4(R)-trans stereoisomeric forms are potent inhibitors of cholesterol synthesis by virtue of their ability to inhibit the enzyme, 3-hydroxy-3-methylglutaryl-coenzyme A reductase.

    专利号:WO-2022200444-A1
    优先权日:2021-03-24
    标 题:New process for the synthesis of 5-{5-chloro-2-[(3n)-3- [(morpholin-4-yl)methyl]-3,4-dihydroisoquinoline-2(1h)- carbonyl]phenyl}-1,2-dimethyl-1h-pyrrole-3-carboxylic acid derivatives and its application for the production of pharmaceutical compounds

    专利号:US-4567289-A
    优先权日:1979-08-17
    标 题 :Substituted pyranone inhibitors of cholesterol synthesis
    发明人:WILLARD ALVIN K; NOVELLO FREDERICK C; HOFFMAN WILLIAM F; CRAGOE JR EDWARD J
    权利人:MERCK & CO INC
    摘要:The methyl, ethyl, n-propy, 2-(acetylamino)ethyl, or 1-(2,3-dihydroxy)propyl ester of E-(3R,5S)-7-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)-3,5-dihyd roxy-6-heptenoic acid of structural formula: are HMG-CoA reductase inhibitors useful in the treatment of conditions associated with hypercholesterolemia.

    专利号:US-9657037-B2
    优先权日:2013-06-03
    标 题:Pyrrole compounds with silicon incorporation
    发明人:REDDY DUMBALA SRINIVASA; VASUDEVAN NATARAJAN; WAGH SACHIN BHAUSAHEB; RAMESH REMYA
    权利人:COUNCIL SCIENT IND RES
    摘要:The present invention discloses novel Silicon incorporated pyrrole compounds of Formula I having potential anti-bacterial properties. The invention further discloses a process for synthesis of pyrrole compounds with silicon incorporation of Formula I and to the pharmaceutical composition thereof.
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    合成参考文献


    摘要:Gribble, G. W., Science of Synthesis, (2006) 8, 362.
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