CAS: 6245-57-4; 4-Methoxy-2-Methylbenzoic Acid

上下游产品

CAS号124-38-9 二氧化碳 | CAS号27060-75-9 2-溴-5-甲氧基甲苯 | CAS号52289-54-0 4-甲氧基-2-甲基苯甲醛 | CAS号100-09-4 对甲氧基苯甲酸 | CAS号74-88-4 碘甲烷 | CAS号201230-82-2 carbon monoxide | CAS号100-84-5 间甲基苯甲醚 | CAS号148706-30-3 4-甲氧基-2-甲基苯基溴化镁 | CAS号24826-74-2 1-(4-甲氧基-2-甲基苯基)乙酮 | CAS号74331-69-4 1-乙炔基-4-甲氧基-2-甲基苯 | CAS号35598-05-1 4-甲氧基-2-甲基苯甲酸甲酯 | CAS号1885-13-8 4-甲氧基邻苯二甲酸 | CAS号610-35-5 4-羟基邻苯二甲酸 | CAS号578-39-2 4-羟基-2-甲基苯甲酸 | CAS号139583-91-8 4-Methoxy-2-met... | CAS号31310-08-4 4-甲氧基-2-甲基苯甲酰氯 | CAS号15365-25-0 2-溴甲基-4-甲氧基苯甲酸甲酯 | CAS号85303-97-5 5-(4-methoxy-2-... | CAS号90359-73-2 N,N-二乙基-4-甲氧基-2... | CAS号942-97-2 4-甲氧基-2-甲基苯乙酸

2-甲基-4-甲氧基苯胺置于sodium Hydroxide,Potassium Permanganate体系中,化学反应生成 4-甲氧基-2-甲基苯甲酸
参考文献:Ortho Substitution Rearrangement Of Certain 3-Substituted And 3,5-Disubstituted Benzyltrimethylammonium Ions By Sodium Amide1
标题:Ortho Substitution Rearrangement Of Certain 3-Substituted And 3,5-Disubstituted Benzyltrimethylammonium Ions By Sodium Amide1
摘要:
DOI:10.1021/jo01351A039

专利信息

专利号:WO-2025019598-A1
优先权日:2023-07-20
标 题:Positive allosteric modulator of the metabotropic glutamate receptor subtype 2 receptor, synthesis and solid forms thereof
发明人：COSFORD NICHOLAS DAVID PETER; SHEFFLER DOUGLAS J
权利人:SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INST
摘要:Described herein are solid forms of sodium 4-chloro-3'-(((2-cyclopentyl-1-oxoisoindolin-5-yl)oxy)methyl)-[1,1'-biphenyl]-3-carboxylate and its pharmaceutical composition for the treatment of disease.

专利号:RU-2585623-C1
优先权日:2014-11-20
标题 :METHOD FOR SYNTHESIS OF 7-METHOXY-4-NITRO-3-(p-METHOXYPHENYL) ISOQUINOLINONE DERIVATIVES

专利号:WO-9314086-A1
优先权日:1992-01-17
标 题 :Substituted 1-isoquinolone derivatives as angiotensin ii antagonists
发明人：FISHER LAWRENCE E; CAROON JOAN M; STABLER STEPHEN R; CLARK ROBIN D
权利人:SYNTEX INC
摘要:1-Isoquinolone derivatives and related compounds according to formula (I) wherein, Y is selected from the group consisting of H, OH, lower alkoxy, and halo; X is selected from the group consisting of H, lower alkyl acid, lower alkyl ester, and lower alkyl; and R1 is selected from the group consisting of H, alkenyl, lower alkyl, lower cycloalkyl, unsubstituted or substituted 3-spiro-1H-indane of structure (II) wherein R2 is H, OH, lower alkyl, lower alkoxy or halo, and 3-spiro-cycloalkyl of structure (III) wherein n is an integer from zero to six, provided that when R1 is spiro- X is H, or a pharmaceutically acceptable salt thereof, with the proviso that when R1 is spiro-, X is H, and when R1 is H, alkenyl, lower alkyl or lower cycloalkyl substituted at the 3-position of the isoquinolone moiety and X is H or lower alkyl, the (2'-1H--tetrazol-5-yl)biphenyl-4'-ylmethyl group cannot be at the 2(N) position, are useful as angiotensin II receptor antagonists. Also disclosed are methods of synthesis, intermediates, pharmaceutical formulations and methods of treatment.

专利号:CN-109053542-A
优先权日:2018-07-25
标题:A kind of chemical synthesis method of 6-bromo-5-hydroxyisoindoline-1-one

专利号:US-8461107-B2
优先权日:2008-04-28
标题:HCV NS3 protease inhibitors
发明人：LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; GILBERT KEVIN F; MCINTYRE CHARLES J; RUDD MICHAEL T
权利人:LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; GILBERT KEVIN F; MCINTYRE CHARLES J; RUDD MICHAEL T; MERCK SHARP & DOHME
摘要:The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.

专利号:WO-2010099503-A1
优先权日:2009-02-26
标题:Compositions, synthesis, and methods of utilizing quinazolinedione derivatives