CAS: 20651-71-2; 4-Butylbenzoic Acid

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CAS号124-38-9 二氧化碳 | CAS号41492-05-1 对丁基溴苯 | CAS号557-20-0 二乙基锌 | CAS号201230-82-2 carbon monoxide | CAS号20651-67-6 1-正-丁基-4-碘苯 | CAS号122-56-5 三丁基硼 | CAS号586-76-5 对溴苯甲酸 | CAS号28788-62-7 4-丁基苯甲酰氯 | CAS号542-69-8 碘代正丁烷 | CAS号65-85-0 苯甲酸 | CAS号10531-16-5 4-丁基苄溴 | CAS号38454-28-3 4-正丁基苯甲酸 4-己氧基苯酯 | CAS号38289-28-0 丁基环己基甲酸 | CAS号20651-69-8 4-丁基苯甲酸甲酯 | CAS号107377-07-1 4-丁基苯甲酰胺 | CAS号35684-23-2 p-Butylbenzoic ... | CAS号28788-62-7 4-丁基苯甲酰氯 | CAS号67589-47-3 反-4-丁基环己烷甲酸4-乙氧基苯酯 | CAS号60834-63-1 对丁基苯甲醇 | CAS号62622-28-0 4’-丁基苯甲酸 4-氰基联苯酯

丁苯置于jones Reagent体系中,用 丙酮,三氟乙酸 用作溶剂,化学反应 0.5H,反应生成4-丁基苯甲酸
参考文献:新的有效的白三烯c4和d4拮抗剂.1.合成与构效关系.
标题:新的有效的白三烯c4和d4拮抗剂.1.合成与构效关系.
摘要:(p-戊基肉桂酰基)邻氨基苯甲酸(3A)对ltd4-诱导的豚鼠回肠平滑肌收缩和ltc4诱导的豚鼠支气管收缩具有中等程度的拮抗活性.对3A的疏水部分(肉桂酰基部分)和亲水部分(邻氨基苯甲酸酯部分)进行了修饰.揭示了一系列的8-(苯甲酰基氨基)-2-四唑-5-基-1,4-苯并二恶烷和8-(苯甲酰基氨基)-2-四唑-5-基-4-氧代-4H-1-苯并吡喃.白三烯c4和d4的有效拮抗剂.在这两个系列中,Ono-Rs-347(18K)和ono-Rs-411(19H)分别是最有效和口服活性的拮抗剂.讨论了构效关系.
Doi:10.1021/jm00396A013

专利信息

专利号:US-6664282-B2
优先权日:1999-09-17
标 题:Synthesis of [3,5,7]-1H-imidazo [1,5-a]imidazol-2 (3H)- one compounds
发明人：ELABDELLAOUI HASSAN M; OSTRESH JOHN M; HOUGHTEN RICHARD A
权利人:TORREY PINES INST
摘要:Individual substituted [3,5,7]-1H-imidazo[1,5-a]imidazol-2(3H)-one compounds and their pharmaceutically-acceptable salts are disclosed, as are libraries of such compounds. Methods of preparing and using the libraries of compounds as well as individual compounds of the libraries are also disclosed.

专利号:US-5856107-A
优先权日:1997-02-04
标 题 :Combinatorial libraries of imidazol-pyrido-indole and imidazol-pyrido-benzothiophene derivatives, methods of making the libraries and compounds therein
发明人：OSTRESH JOHN M; HOUGHTEN RICHARD A
权利人:TREGA BIOSCIENCES INC
摘要:The invention provides a rapid approach for combinatorial synthesis and screening of libraries of imidazol-pyrido-indole and imidazol-pyrido-benzothiophene compounds. The present invention further provides methods of preparing the libraries and the individual compounds made by the combinatorial synthesis.

专利号:US-7468130-B2
优先权日:2005-02-15
标题 :Organosilanes and substrates covalently bonded with same and methods for synthesis and use same
发明人：LIU XIAODONG; POHL CHRISTOPHER A
权利人:DIONEX CORP
摘要:The present invention provides novel silicon compounds, methods for making these novel silicon compounds, compositions comprising these novel silicon compounds attached to substrates, methods for attaching the novel silicon compounds to substrates and methods for using the compositions in a variety of chromatographic applications.

专利号:US-9662318-B2
优先权日:2012-07-16
标题 :Bitopic muscarinic agonists and antagonists and methods of synthesis and use thereof
发明人：BOULOS JOHN
权利人:BARRY UNIV INC
摘要:Compositions for treating a condition associated with activity of a muscarinic receptor (e.g., one or more of M 1 , M 2 , M 3 , M 4 , M 5 ) and for anesthetizing a subject include a bitopic muscarinic antagonist or agonist. A bitopic muscarinic antagonist named JB-D4 was discovered. Additional bitopic muscarinic antagonists discovered and described herein include BK-23, HD-42, HD153, HD-185, KH-5, JM-31 and JM-32. These bitopic ligands and their structural analogs, as well as bitopic muscarinic agonists, may be used as neuromuscular blocking agents (e.g., for use in compositions for anesthetizing a subject) and for the treatment of central nervous system disorders (e.g., Parkinson's disease, Schizophrenia, etc.), Overactive Bladder Syndrome, Chronic Obstructive Pulmonary Disease, asthma, and many other diseases associated with the activation or inhibition of M 1 -M 5 acetylcholine receptors.

专利号:RU-2026854-C1
优先权日:1991-02-07
标题:Method of synthesis of p-butylbenzoic acid

专利号:WO-0119783-A1
优先权日:1999-09-17
标 题:Synthesis of [3,5,7]-1h-imidazo[1,5-a]imidazol-2(3h)-one compounds