CAS: 2486-80-8; 4-Amino-2-Methoxybenzoic Acid

上下游产品

CAS号2597-56-0 2-甲氧基-4-硝基苯甲酸 | CAS号27492-84-8 2-甲氧基-4-氨基苯甲酸甲酯 | CAS号4093-29-2 胃复安甲基物 | CAS号39106-79-1 2-甲氧基-4-硝基苯甲酸甲脂 | CAS号101084-96-2 2-甲氧基-4-硝基苯甲腈 | CAS号6059-17-2 4-AMINO-2-HYDRO... | CAS号65-49-6 对氨基水杨酸 | CAS号55304-05-7 4-acetylamino-2... | CAS号1134-65-2 2-methoxy-4-ace... | CAS号27492-84-8 2-甲氧基-4-氨基苯甲酸甲酯 | CAS号102361-94-4 Benzoyl chlorid... | CAS号3614-38-8 4-(acetylamino)... | CAS号155928-39-5 4-Amino-5-iodo-... | CAS号3761-48-6 4-氨基-N-[2-(二乙基氨... | CAS号72856-73-6 2-甲氧基-4-(甲硫基)苯甲酸 | CAS号89469-44-3 2-甲氧基-4-[(甲基磺酰基... | CAS号89469-52-3 4-氰基-2-甲氧基苯甲酸

4-氨基水杨酸置于硫酸,水,Potassium Carbonate,Sodium Hydroxide体系中,用 甲醇,乙醇,丙酮 用作溶剂,化学反应 17.5H,反应生成4-氨基-2-甲氧基苯甲酸
参考文献:水杨酸衍生物作为基于镧系元素配比的发光探针的天线.
标题:水杨酸衍生物作为基于镧系元素配比的发光探针的天线.
摘要:长寿命比例传感器:发光镧系元素络合物广泛用于生物分子的时间分辨测定中,但是大多数具有这些络合物的传感器都依赖于单点强度测量.在这里,我们介绍一种简单的策略,通过使用水杨酸衍生物作为tb 3+配合物的天线部分来创建比例探针.例如,开发了碱性磷酸酶(alp)的探针(参见方案).
Doi:10.1002/chem.201200610

专利信息

专利号:US-2012165520-A1
优先权日:2010-12-23
标题:Process for the synthesis of prodrugs of opioids
发明人：MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
权利人:MCGEE PAUL; GARNETT IAN; JUAN E; MANAGE A; CARNIAUX JEAN-FRANCOIS
摘要:The present invention provides a process for the synthesis of opioid prodrugs. In particular, the present invention provides a process for the synthesis of opioid prodrugs comprising: treating an opioid, in the form of a salt or a freebase, with a carbonyl synthon to form an activated intermediate and subsequently reacting the activated intermediate with an amine, in the form of a salt or a freebase.

专利号:US-7550510-B2
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides
发明人：CURLEY JR ROBERT W; MERSHON SERENA M; BARNETT DEREK W; CLAGETT-DAME MARGARET; CHAPMAN JASON S
权利人:WISCONSIN ALUMNI RES FOUND
摘要:A solid phase synthetic method for preparing arylretinamides is provided. The method comprises reacting hexachloroacetone with a solvent-suspended resin-bound triphenylphosphine to provide a suspension comprising an activated chlorinating reagent; reacting retinoic acid with the activated chlorinating reagent to provide retinoyl chloride; adding pyridine and a select arylamine to the resulting mixture; and stirring the resulting mixture for a time and at a temperature sufficient for the select arylamine to react with the retinoyl chloride and provide the arylretinamide. Also provided, are select arylretinamides that can be prepared by the present method, and methods of using such arylretinamides to induce apoptosis in cancer cells.

专利号:US-2004102650-A1
优先权日:2001-07-06
标 题:Solid phase synthesis of arylretinamides

专利号:US-2003105164-A1
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides

专利号:WO-03003987-A2
优先权日:2001-07-06
标题:Solid phase synthesis of arylretinamides

专利号:US-6696606-B2
优先权日:2001-07-06
标 题 :Solid phase synthesis of arylretinamides