CAS: 5962-41-4; 2-Phosphonopropanoic Acid

该化合物是一种有机磷磷酸化合物,其特点是存在一种磷酸功能组,该化合物具有三碳链,与附于第二碳的磷酸组有三碳联系,具有独特的化学特性,通常无色可粉黄黄色液体或固体,视其形态和纯度而定.

结构式图片

相似化合物

4378-40-9 4408-78-0 40962-37-6

上下游产品

methyl 2-(diethoxyphosphoryl)propanoate ethyl 2-diethoxyphosphorylpropionate

合成工艺路线路线简述

    📜三乙基2-膦酰基丙酯 以 盐酸 作为反应溶剂,化学反应 3.0H,以to Yield 2-Phosphonopropionic Acid (Quantitative)的收率获得产物2-膦酰基丙酸
    参考文献:Phosphonoacyl Prolines And Related Compounds
    标题:Phosphonoacyl Prolines And Related Compounds
    摘要:新的磷酸酰脯氨酸和相关化合物的一般结构式为##str1## 其中r.Sub.1和r.Sub.2分别为氢,低碳基,低烯基,未取代或取代的苯基-低碳基或金属离子;r.Sub.3为氢或低碳基;r.Sub.4为氢,低碳基,苯基-低碳基或金属离子;n为0或1.这些化合物可用作降压剂.

    海关参考信息

    专利信息


    专利号:EP-0468457-B1
    优先权日:1990-07-24
    标题 :Novel substituted piperidines and their use as inhibitors of cholesterol synthesis
    发明人:MCCARTHY JAMES R; BARNEY CHARLOTTE L; WANNAMAKER MARION W
    权利人:MERRELL DOW PHARMA
    摘要:The present invention relates to a group of compounds which are novel substituted piperidines and which act to inhibit the synthesis of cholesterol in mammals and in fungi.

    专利号:US-4539410-A
    优先权日:1982-09-30
    标题:N-Substituted-2-(1-imidazolyl)indoles
    发明人:RENFROE HARRIS B
    权利人:CIBA GEIGY CORP
    摘要:Various 1-carboxylic acid substituted-2-(1-imidazolyl)indoles and functional derivatives thereof are highly specific thromboxane synthetase inhibitors. Synthesis of, pharmaceutical compositions thereof, methods of treatment utilizing such compounds and intermediates for their synthesis are included.

    专利号:US-6140515-A
    优先权日:1997-09-24
    标题 :Process of making 3-aryloxy, 4-aryl furan-2-ones useful as inhibitors of COX-2
    发明人:CHEN CHENG Y; TAN LUSHI; LARSEN ROBERT D
    权利人:MERCK & CO INC
    摘要:Described is a process of preparing 3-aryl, 4-aryloxy furan-5-ones which are useful as inhibitors of cyclooxygenase-2 (COX-2). Such compounds are useful as anti-inflammatory agents. The process is directed to an asymmetric synthesis which involves: a trisubstituted styrene derivative preparation via Horner-Wadsworth-Emmons reaction and subsequent one pot trifluoromethylation of the allylic alcohol; preparation of the alpha -hydroxyl ketone using Sharpless asymmetric dihydroxylation and Swern oxidation; the esterification of the alpha -hydroxyl ketone with the phenoxy acetic acid; and the Dieckman condensation of the resulting ester.

    专利号:US-7973109-B2
    优先权日:2007-03-29
    标 题 :Crosslinked type layered metal phosphonate compound, production process therefor, non-crosslinked type layered metal phosphonate compound, production process therefor, as well as stock solution
    发明人:OGATA SHIN-ICHI; FUKUSHIMA YOSHIAKI; KAWASUMI MASAYA
    权利人:TOYOTA CHUO KENKYUSHO KK
    摘要:A process for producing a crosslinked type or non-crosslinked type layered metal phosphonate compound including a reaction step of reacting two or more members selected from organic diphosphonic acids or monophosphonic acids, or derivatives thereof having predetermined conditions and a metal source capable of forming an ion of a hexacoordinate metal atom as a central atom (M) of a metal oxide octahedron upon reaction under the presence of a sulfuric acid catalyst, a crosslinked or non-crosslinked metal phosphonate compound obtained by the process, as well as a stock solution used for the synthesis of the crosslinked or non-crosslinked type layered metal phosphonate compound described above.

    专利号:US-7420070-B2
    优先权日:2000-12-28
    标 题:Process for preparing optically active 2,3-dihydrobenzofuran compounds
    发明人:AOKI ISAO; ADACHI MARI; TAWADA HIROYUKI; YAMASHITA MAKOTO; SERA MISAYO
    权利人:TAKODA PHARMACEUTICAL COMPANY
    摘要:A process for preparing optically active 2,3-dihydrobenzofuran compounds which comprises subjecting a 2,3-dihydrobenzofuran compound represented by the general formula or a salt thereof to optical resolution with an optically active acid compound: n n[wherein R 1 and R 2 are each hydrogen or an optionally substituted hydrocarbon group; R 3 is an optionally substituted aromatic group; and C is a benzene ring which may further have a substituent in addition to the amino group]. The process enables industrially advantageous production of intermediates for the synthesis of optically active 2,3-dihydrobenzofuran compounds useful as preventive and/or therapeutic drugs for neurodegenerative diseases and so on.

    专利号:US-2012164231-A1
    优先权日:2009-08-25
    标题 :Synthesis Of Oxygen Carrying, Turbulence Resistant, High Density Submicron Particulates

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    合成参考文献


    参考文献:10.1023/a:1014409929875
    摘要:Kononova SV, Nesmeyanova MA. Phosphonates and their degradation by microorganisms. Biochemistry (Mosc). 2002 Feb;67(2):184–95. doi: 10.1023/a:1014409929875.
    参考文献:10.1007/bf02994766
    摘要:Hong JH. Synthesis and antiviral evaluation of novel 3'- and 4'-doubly branched carbocyclic nucleosides as potential antiviral agents. Arch Pharm Res. 2003 Dec;26(12):1109–16. doi: 10.1007/bf02994766.
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