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    • 3. 发明授权
    • Haloethersilanes
    • 卤代硅烷
    • US3334123A
    • 1967-08-01
    • US31487963
    • 1963-10-09
    • DOW CORNING
    • CULPEPPER ALAN L
    • C07F7/08C07F7/12C07F7/18C08G77/00C08G77/04C08G77/24D06M13/513D06M15/643
    • D06M13/513C07F7/0852C07F7/0854C07F7/0892C07F7/12C07F7/1828C07F7/1896C08G77/00C08G77/04C08G77/24D06M15/6436
    • Chloromethylallyl ether is prepared by passing anhydrous hydrogen chloride into an equimolar mixture of allyl alcohol and paraformaldehyde; the water layer is then removed and excess acid blown off with nitrogen (see Example 1).ALSO:The invention comprises (1) haloether silanes of formula XC(H)(R1)-OR-SiQQ1Q11; (2) haloether-siloxanes containing units of formula with or without units of formula ; and (3) the quaternary ammonium salts thereof; wherein Q, Q1 and Q11 are each a hydrogen or halogen atom, a hydroxy monovalent hydrocarbon or halohydrocarbon radical which is free from aliphatic unsaturation, or a radical of formula bRO-, bR-COO-, bR2C=N-O-, bR=C=N-O- or R11O(CH2CH2O)m-, where bR is a hydrocarbon or a halohydrocarbon radical, R11 is an alkyl radical containing 1 to 4 carbon atoms, m is 1 or 2, R is a divalent aliphatic or cycloaliphatic hydrocarbon radical containing more than one carbon atom, R1 is a hydrocarbon radical containing 1 to 6 carbon atoms or a hydrogen atom, X is a halogen atom, n is 0-2, a is 0-3, Y is an H, hydrocarbon, halohydrocarbon, alkoxy, acyloxy, phenoxy, isocyanoxy, or hydroxy radical. The quaternary ammonium salts are derived from tertiary amines containing not more than one aromatic group. The haloether silanes may be prepared by the addition of HSiQQ1Q11 to XCH(R1)-O-W, where W is a monovalent unsaturated aliphatic or cycloaliphatic hydrocarbon carbon radical. These may be hydrolysed or cohydrolysed to the corresponding haloether siloxanes. The quaternary ammonium silanes and siloxanes may be prepared by mixing the corresponding haloether silane or siloxane with the appropriate tertiary amine; quaternary ammonium siloxanes may also be prepared by the hydrolysis of the corresponding quaternary ammonium silanes. Many examples are given: typical examples describe the preparation of (1) ClCH2O(CH2)3Si(CH3)Cl2; (2) the siloxane therefrom of unit formula ClCH2O(CH2)3Si(CH3)O-; (6) the pyridine salt thereof of formula and (9) a quaternary ammonium siloxane copolymer comprising units of formulae (CH3)2SiO, (CH3)SiO3/2 and Uses.-Waterproofing fabrics.ALSO:Fabrics are treated with a siloxane copolymer comprising (1) 0.5 to 50 mole per cent of (a) halo-ether siloxane units of formula XCH(R')-OR-Si(Q)n , and/or the quaternary ammonium salts thereof (2) 99.5 to 50 mole per cent of units of formula ; wherein, X is a halogen atom, R is a divalent aliphatic or cycloaliphatic hydrocarbon radical containing more than one carbon atom, R' is hydrogen or a monovalent hydrocarbon radical containing 1 to 6 carbon atoms, Q is a hydrogen or halogen atom or a hydroxy or monovalent hydrocarbon or halohydrocarbon radical free from aliphatic unsaturation, or a radical of formula or R"O(CH2CH2O)m-, wherein R is a hydrocarbon or halohydrocabon radical, n is 0-2, m is 1 or 2, a is 0-3 and Y is an H, hydrocarbon, halohydrocarbon, alkoxy, acyloxy, phenoxy, hydrocarbyl-substituted isocyanoxy or hydroxy radical. These siloxanes may be used per se or in admixture with conventional siloxane water-repellents. Cellulose fabrics are prefered. The siloxanes are preferably applied in the form of emulsion or in solution, preferably with a curing agent e.g. metal carboxylates or alkanol amine titanates. Examples 11, 12 and 18 describe the treatment of cotton fabrics with various siloxanes.
    • 4. 发明申请
    • PURIFICATION OF SYNTHETIC OLIGONUCLEOTIDES
    • 合成寡核苷酸的纯化
    • WO2012047639A3
    • 2012-06-28
    • PCT/US2011053429
    • 2011-09-27
    • UNIV MICHIGAN TECHFANG SHIYUE
    • FANG SHIYUE
    • C07H21/00
    • C07H21/00C07F7/1828C07F9/222C07H1/06C07H19/073C07H19/10C07H23/00
    • This invention provides a method for purifying synthetic oligonucleotides comprising capping, polymerizing and separating any failure sequences produced during oligonucleotide synthesis. The invention also provides a method for purifying synthetic oligonucleotides comprising reacting a full length oligonucleotide with a compound to attach a polymerizable functional group to an end of the full length oligonucleotide, polymerizing the full length oligonucleotides and removing the failure sequences, and recovering the full length oligonucleotides. The invention also provides novel capping agents having a polymerizable functional group, and kits comprising at least one composition of the present invention.
    • 本发明提供了纯化合成寡核苷酸的方法,其包括封端,聚合和分离在寡核苷酸合成期间产生的任何失效序列。 本发明还提供了纯化合成寡核苷酸的方法,其包括使全长寡核苷酸与化合物反应以将可聚合官能团连接到全长寡核苷酸的末端,聚合全长寡核苷酸并除去失败序列,并回收全长 寡核苷酸。 本发明还提供了具有可聚合官能团的新型封端剂和包含至少一种本发明组合物的试剂盒。
    • 10. 发明授权
    • Organosilane esters having glycol ether moieties
    • 具有乙二醇醚部分的有机硅烷酯
    • US4551541A
    • 1985-11-05
    • US462863
    • 1983-02-01
    • Horst Hanisch
    • Horst Hanisch
    • C07F7/18C09K3/10C07F7/08C07F7/10
    • C09K3/1021C07F7/1828C09K2200/0239C09K2200/0247
    • The present invention relates to new organosilane esters which can be characterized by the formula Y-(CH.sub.2).sub.n Si(CH.sub.3).sub.p -X.sub.m Z.sub.3-(m+p). In this formula, Y represents either a substituted or unsubstituted amino group, or it represents the mercapto moiety or the moiety ##STR1## X represents an alkoxy group with 1 to 4 carbon atoms and Z a glycol ether moiety. The index n can assume the numerical values from 1 to 3, m can be 0 or 1 and p can be 0 or 1 or 2, on the condition that m+p is equal to or less than 2. The new silanes yield very stable hydrolyzates and have good adhesion-improving properties. They are therefore particularly well suited for use in sealing compositions.
    • 本发明涉及可由式Y-(CH 2)n Si(CH 3)p -X m Z 3 - (m + p)表征的新的有机硅烷酯。 在该式中,Y表示取代或未取代的氨基,或表示巯基部分或部分X表示具有1至4个碳原子的烷氧基,Z表示乙二醇醚部分。 索引n可以假设从1到3的数值,m可以是0或1,p可以是0或1或2,条件是m + p等于或小于2.新的硅烷产生非常稳定 水解并具有良好的粘附性改善性能。 因此,它们特别适用于密封组合物。