CAS: 56-35-9; Tributyltin Oxide

上下游产品

tributyltin chloride tributylethynyltin μ-oxobis[(trifluoromethanesulfonato)(phenyl)iodine] β-(cyclohexylthio)ethyl tri-n-butyltin sulfidetributyl(1-chloro-3-phenoxy-2-propanyloxy)stannane Acetic acid (2S,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{4-[4-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-phenylethynyl]-phenoxy}-tetrahydro-pyran-3-yl ester 5-(3,5-Dichlorophenylthio)-4-isopropyl-1-methyl-2-(N-methylcarbamoyl)oxymethyl-1H-imidazole 3-Phenoxycarbonyl-3,4,5,6-tetrahydro-2H-1,3-oxazin-2-one

Diphenylphosphinigsaeure-Tri-N-Butylstannylester置于naoh体系中,化学反应生成 三丁基氧化锡
参考文献:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Sn: Org.Comp.12,1.4.1.1.1.5.14,Page 215-220
标题:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Sn: Org.Comp.12,1.4.1.1.1.5.14,Page 215-220

专利信息

专利号:US-9096647-B2
优先权日:2008-09-16
标题 :Simplified one-pot synthesis of [18F]SFB for radiolabeling
发明人：OLMA SEBASTIAN; SHEN CLIFTON KWANG-FU
权利人:UNIV CALIFORNIA
摘要:A non-aqueous single pot synthesis of [ 18 F]SFB is set forth. The [ 18 F]SFB produced with this method is then used, for example, to label a peptide or an engineered antibody fragment (diabody) targeting human epidermal growth factor receptor 2 (HER2) as representative examples of labeled compounds for use as an injectable composition to locate abnormal tissue, specifically tumors within an animal or human using a PET scan.

专利号:US-2010098623-A1
优先权日:2007-02-07
标 题 :Zeolite materials and synthesis method thereof
发明人：GAGEA BOGDAN; JACOBS PIERRE; MARTENS JOHAN; VANDEPITTE HANS
权利人:GAGEA BOGDAN; JACOBS PIERRE; MARTENS JOHAN; VANDEPITTE HANS
摘要:The present invention provides zeolites and zeolite-like material having an enhanced microporosity. It was found that such zeolites can be obtained using a zeolite synthesis method comprising the preparation of a gel or solution for the synthesis of a zeolite, said gel or solution comprising appropriate amounts of (i) a conventional monomeric or polymeric silica source and (ii) a molecular template as a microstructuring agent, characterized in that said gel or solution further comprises an organosilane compound having limited self-assembling capacity.

专利号:US-8987430-B2
优先权日:2009-10-30
标 题:Efficient and scalable process for the manufacture of fondaparinux sodium
发明人：PATEL PAYAL PARTH; MA CHUN; OHRR KEVIN K; NADJI SOURENA
权利人:PATEL PAYAL PARTH; MA CHUN; OHRR KEVIN K; NADJI SOURENA; RELIABLE BIOPHARMACEUTICAL CORP
摘要:The present invention relates to a process for the synthesis of the Factor Xa anticoagulent Fondaparinux and related compounds. The invention relates, in addition, to efficient and scalable processes for the synthesis of various intermediates useful in the synthesis of Fondaparinux and related compounds.

专利号:US-11465129-B2
优先权日:2017-06-06
标题:Microwave assisted and low-temperature fabrication of nanowire arrays on scalable 2D and 3D substrates
发明人：GAO PU-XIAN; LU XINGXU; HOANG SON
权利人:UNIV CONNECTICUT
摘要:A method of making a titanium dioxide nanowire array includes contacting a substrate with a solvent comprising a titanium (III) precursor, an acid, and an oxidant while microwave heating the solvent, thereby forming a hydrogen titanate H2Ti2O5.H2O nanowire array. The hydrogen titanate nanowire array is annealed to form a titanium dioxide nanowire array. The substrate is seeded with titanium dioxide before starting the hydrothermal synthesis of the hydrogen titanate nanowire array. The titanium dioxide nanowire array is loaded with a platinum group metal to form an exhaust gas catalyst. The titanium dioxide nanowire array can be used to catalyze oxidation of combustion exhaust.

专利号:US-2021163438-A1
优先权日:2017-08-16
标题 :Synthesis of phytocannabinoids including a demethylation step
发明人：REEKIE TRISTAN; SCOTT MICHAEL; KASSIOU MICHAEL
权利人:UNIV SYDNEY
摘要:A method for demethylating a methylated phytocannabinoid compound of Formula I to form a phytocannabinoid compound of Formula II: Formula I Formula II wherein: R1 is selected from the group consisting of: substituted or unsubstituted C1-C5 alkyl; R2 is selected from the group consisting of: OH or O, and R3 is selected from the group consisting of: a substituted or unsubstituted cyclohexene, a substituted or unsubstituted C2-C8 alkene, or a substituted or unsubstituted C2-C8 dialkene; or R2 is O, and R2 and R3 together form a ring structure in which R2 is an internal ring atom; wherein the method includes: heating a reaction mixture comprising the methylated phytocannabinoid compounds and a polar aprotic solvent in the presence of a dissolved inorganic alkaline salt for a time sufficient to demethylate at least a portion of the methylated phytocannabinoid compounds and form the phytocannabinoid compound.

专利号:US-6544952-B1
优先权日:1994-03-15
标 题:Synthesis of glycoconjugates of the globo-H epitope and uses thereof
发明人：DANISHEFSKY SAMUEL J; LIVINGSTON PHILIP O; RAGUPATHI GOVINDASWAMI; KIM IN JONG; SCHER HOWARD; SLOVIN SUSAN
权利人:SLOAN KETTERING INST CANCER
摘要:The present invention provides a method of synthesizing a compound having the structure:as well as other related glycoconjugates useful as vaccines for inducing antibodies to epithelial cancer cells in an adjuvant therapy therefore, and in a method for preventing recurrence of epithelial cancer. The present invention also provides a vaccine comprising an amount of the compound described above effective to prevent the recurrence of cancer in a subject.