CAS: 85317-52-8; Methyl 2-Amino-3-(4-Nitrophenyl)Propionate

该化合物是一种属于氨基酸衍生物类别的有机化合物,具有甲酯功能组,有助于有机溶剂中的溶性;该化合物含有一个4硝基苯组,其特征是联苯环中存在一个硝基组(-NO2),具有重要的电子特性和潜在的再活性;这种硝基替代可增强该化合物参与生物化学替代反应的能力;甲基四硝基苯乙酸因其结构上与天然氨基酸相似,通常用于生物化学应用,特别是涉及酶活动和蛋白相互作用的研究;其特性,如熔点,沸点和溶性,可因样品的具体条件和纯度而不同;与许多有机化合物一样,在处理该物质时应采取安全防范措施,因为如果浸泡或吸入,可能会对健康造成危害.

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122079-30-5 17193-40-7 67877-95-6

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CAS号67-56-1 甲醇 | CAS号1991-83-9 4-nitrophenylalanine | CAS号17193-40-7 (S)-4-硝基苯基丙氨酸甲酯盐酸盐

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    专利信息


    专利号:US-5135737-A
    优先权日:1986-11-10
    标 题:Amplifier molecules for enhancement of diagnosis and therapy
    发明人:KEANA JOHN F W
    权利人:OREGON STATE
    摘要:Disclosed are amplifier molecules: various organic compounds having branched structures terminating with amine groups to which pharmacologically active groups can be chemically attached. A number of MRI contrast-enhancing agents were synthesized, each comprising plural active groups, such as stable nitroxides and complexes of trivalent metal cations. Such syntheses were successfully performed using a number of amplifiers having different branched structures, demonstrating the general utility of the pertinent chemistry in the synthesis of amplifiers having any of a wide variety of pharmacologically active groups. Amplifiers were also synthesized having linkers terminating with chemically reactive groups such as isothiocyanates, which render the amplifier bifunctional: attachable to polymers, biomacromolecules, or other biocompatible entity possessing multiple reactive sites such as terminal amines. Via such chemistry, the amplifiers are attachable to monoclonal antibodies for concentration of pharmacologically active groups at a desired site in the body.

    专利号:WO-9403593-A1
    优先权日:1992-08-04
    标题 :Amplifier molecules for enhancement of diagnosis and therapy
    发明人:KEANA JOHN F W
    权利人:OREGON STATE
    摘要:Disclosed are amplifier molecules: various organic compounds having branched structures terminating with amine groups to which pharmacologically active groups can be chemically attached. A number of MRI contrast-enhancing agents were synthesized, each comprising plural active groups, such as stable nitroxides and complexes of trivalent metal cations. Such syntheses were successfully performed using a number of amplifiers having different branched structures, demonstrating the general utility of the pertinent chemistry in the synthesis of amplifiers having any of a wide variety of pharmacologically active groups. Amplifiers were also synthesized having linkers terminating with chemically reactive groups such as isothiocyanates, which render the amplifier bifunctional: attachable to polymers, biomacromolecules, or other biocompatible entity possessing multiple reactive sites such as terminal amines. Via such chemistry, the amplifiers are attachable to monoclonal antibodies for concentration of pharmacologically active groups at a desired site in the body.

    专利号:US-6303791-B1
    优先权日:1995-08-07
    标题 :One pot synthesis of 2-oxazolidinone derivatives
    发明人:PATEL RAJNIKANT
    权利人:ZENECA LTD
    摘要:The invention provides an improved process for preparing compounds of formula (I

    专利号:US-5412148-A
    优先权日:1986-11-10
    标题:Amplifier molecules derived from diethylene triaminepentaacetic acid for enhancement of diagnosis and therapy
    发明人:KEANA JOHN F W
    权利人:OREGON STATE
    摘要:Disclosed are amplifier molecules: various organic compounds having branched structures terminating with amine groups to which pharmacologically active groups can be chemically attached. A number of MRI contrast-enhancing agents were synthesized, each comprising plural active groups, such as stable nitroxides and complexes of trivalent metal cations. Such syntheses were successfully performed using a number of amplifiers having different branched structures, demonstrating the general utility of the pertinent chemistry in the synthesis of amplifiers having any of a wide variety of pharmacologically active groups. Amplifiers were also synthesized having linkers terminating with chemically reactive groups such as isothiocyanates, which render the amplifier bifunctional: attachable to polymers, biomacromolecules, or other biocompatible entity possessing multiple reactive sites such as terminal amines. Via such chemistry, the amplifiers are attachable to monoclonal antibodies for concentration of pharmacologically active groups at a desired site in the body.

    专利号:US-6084103-A
    优先权日:1995-08-07
    标题 :One pot synthesis of 2-oxazolidinone derivatives

    专利号:US-8338565-B2
    优先权日:2008-08-20
    标 题 :Macrocyclic compounds for inhibition of tumor necrosis factor alpha
    发明人:LEE JINBO; BOND JULIAN F; TERRETT NICHOLAS; FAVALORO JR FRANK G; WANG DANIEL; BRIGGS TIMOTHY F; SEIGAL BENJAMIN ADAM; SUN WEI-CHUAN; HALE STEPHEN P
    权利人:LEE JINBO; BOND JULIAN F; TERRETT NICHOLAS; FAVALORO JR FRANK G; WANG DANIEL; BRIGGS TIMOTHY F; SEIGAL BENJAMIN ADAM; SUN WEI-CHUAN; HALE STEPHEN P; ENSEMBLE THERAPEUTICS CORP
    摘要:Disclosed herein are macrocyclic compounds and methods for their synthesis and use. In particular, macrocyclic compounds are disclosed that modulate the activity of tumor necrosis factor alpha and/or are useful in the treatment of medical conditions, such as, rheumatoid arthritis, psoriasis, and asthma.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Łaźny, R.; Nodzewska, A., Science of Synthesis Knowledge Updates, (2012) 3, 470.
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