CAS: 66470-81-3; Tris(1,1,1,3,3,3-Hexafluoro-2-Propyl)Phosphite

该化合物是磷酸盐酯,其独特结构包括附于磷原子的三个六氟-2-丙基组,其特点是该化合物具有较高的热稳定性和耐氧化性,因此适合用作各种聚合物配方中的阻燃剂和稳定剂;多种氟化组的存在具有疏水特性,并增加了其化学惰性,这在恶劣条件下有利于需要耐久的用途;此外,该化合物的挥发性较低,有助于其长期应用的有效性;其合成通常涉及三氯化磷与六氟-二-丙醇的反应,导致形成磷酸酯;由于其特殊性能,在电子,涂层和塑料等行业使用磷酸三(1,1,1,3,3,3-六氟2-丙基),其性能和稳定性至关重要;在任何化学物质处理和接触准则方面,都应参考安全数据.

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CAS号920-66-1 六氟异丙醇 | CAS号66559-58-8 dichloro-tris(1...

合成工艺路线路线简述

  • 合成目标产物 Tris(1,1,1,3,3,3-Hexafluoro-2-Propyl) Phosphite 主要起始原料 1,1,1,3,3,3-Hexafluoro-2-Propanol
  • (文献来源)合成步骤主要原料 1,1,1,3,3,3-Hexafluoro-2-Propanol
📜六氟异丙醇置于三乙胺,三氯化磷体系中,用73%的收率获得产物三(1,1,1,3,3,3-六氟-2-丙基)亚磷酸
参考文献:通过h-膦酸酯方法在寡聚脱氧核糖核苷酸合成中使用新的膦酰化和偶联剂
标题:通过h-膦酸酯方法在寡聚脱氧核糖核苷酸合成中使用新的膦酰化和偶联剂
摘要:使用三(1,1,1,3,3,3-六氟-2-丙基)亚磷酸酯作为膦酰化试剂来制备核苷3'-H-膦酸酯单元.还详细讨论了使用新型偶联剂1,3-二甲基-2-氯-咪唑啉鎓氯化物(dmci)通过h-膦酸酯方法形成核苷酸间h-膦酸酯键的方法.
DOI:10.1016/s0040-4039(01)93898-5

海关参考信息

专利信息


专利号:US-5134228-A
优先权日:1988-09-29
标题:Nucleoside-3'-phosphites for synthesis of oligonucleotides
发明人:TAKAKU HIROSHI
权利人:CENTRAL GLASS CO LTD
摘要:The invention provides novel phosphites represented by the general formula (I) and nucleoside-3'-phosphite derivatives represented by the general formula (III). n n (RO).sub.3 P (I) n n wherein R is, for example, a fluoroalkyl group or a substituted phenyl group. ##STR1## wherein R is the same as in (I), R' is a protecting group such as dimethoxytrityl group, and B represents a base, e.g. thymine. n A phosphite (I) is prepared by reacting an alcohol ROH with PCl 3 in the presence of a tertiary amine, and a nucleoside-3'-phosphite (III) is prepared by reacting a phosphite (I) with a nucleoside in a solvent in the presence of a tertiary amine. Phosphites (I) are very stable. Using a nucleoside-3'-phosphite (III) an oligonucleotide can be synthesized on a solid support by a simplified process.

专利号:EP-1112281-B1
优先权日:1998-09-08
标 题:Pteridine nucleotide analogs
发明人:HAWKINS MARY E; PFLEIDERER WOLFGANG; BALIS FRANK
权利人:US GOV HEALTH & HUMAN SERV
摘要:The invention provides pteridine nucleotides of formula (I) which are highly fluorescent and which can be used in the chemical synthesis of fluorescent oligonucleotide. The invention further provides for fluorescent oligonucleotide comprising one or more pteridine nucleotides. In addition the invention provides for pteridine nucleotide triphosphates which may be used as the constituent monomers in DNA amplification procedures. The pteridine nucleotides are more stable and possess higher quantum yields than structurally similar pteridine nucleotides.

专利号:US-9273084-B2
优先权日:2012-04-06
标 题 :Moenomycin analogs, methods of synthesis, and uses thereof
发明人:KAHNE DANIEL EVAN; KAHNE SUZANNE WALKER; TSUKAMOTO HIROKAZU
权利人:HARVARD COLLEGE
摘要:The present invention provides compounds of Formula (I); or a pharmaceutically acceptable form thereof; wherein R 1 ,R 2 ,R 3 ,R 6 ,R 7 ,R 12 ,R a , and R b are as defined herein, and G is a group of Formula (a), (b), or (c): Formula (II), wherein X 1 ; X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , Y, R C , R d , R z , a, d, e, x, n, and m are as defined herein. The present invention further provides pharmaceutical compositions comprising a compound of Formula (I), kits comprising such compositions, methods of use and treatment, and preparative methods.

专利号:US-6716971-B1
优先权日:1998-09-08
标题:Pteridine nucleotide analogs
发明人:HAWKINS MARY E; PFLEIDERER WOLFGANG; BALIS FRANK
权利人:US HEALTH
摘要:The invention provides pteridine nucleotides of formula (I) which are highly fluorescent and which can be used in the chemical synthesis of fluorescent oligonucleotide. The invention further provides for fluorescent oligonucleotide comprising one or more pteridine nucleotides. In addition the invention provides for pteridine nucleotide triphosphates which may be used as the constituent monomers in DNA amplification procedures. The pteridine nucleotides are more stable and possess higher quantum yields than structurally similar pteridine nucleotides.

专利号:DE-3932471-A1
优先权日:1988-09-29
标题 :NEW PHOSPHITE AND NUCLEOSIDE-3'-PHOSPHITE FOR THE SYNTHESIS OF OLIGONUCLEOTIDES

专利号:US-5612468-A
优先权日:1994-05-18
标题:Pteridine nucletide analogs as fluorescent DNA probes
发明人:HAWKINS MARY E; PFLEIDERER WOLFGANG; DAVIS MICHAEL D; BALIS FRANK
权利人:US HEALTH
摘要:The invention provides novel pteridine nucleotides which are highly fluorescent under physiological conditions and which may be used in the chemical synthesis of fluorescent oligonucleotides. The invention further provides for fluorescent oligonucleotides comprising one or more pteridine nucleotides. In addition the invention provides for pteridine nucleotide triphosphates which may be used as the constituent monomers in DNA amplification procedures.

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合成参考文献


摘要:Harris, P. A., Science of Synthesis: Knowledge Updates, (2024) 1, 71.
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