CAS: 112-61-8; Methyl Stearate

相似化合物

112-92-5 638-66-4 57-11-4

上下游产品

CAS号112-62-9 油酸甲酯 | CAS号67-56-1 甲醇 | CAS号57-11-4 硬脂酸 | CAS号822-16-2 硬脂酸钠 | CAS号638-08-4 硬脂酸酐 | CAS号77-76-9 2,2-二甲氧基丙烷 | CAS号301-00-8 亚麻酸甲酯 | CAS号25456-04-6 METHYL 9,10-DIB... | CAS号2462-84-2 反油酸甲酯 | CAS号35599-78-1 1-iodopentadecane | CAS号67-56-1 甲醇 | CAS号109-36-4 十八烷酸辛酯 | CAS号4130-54-5 硬脂酰肼 | CAS号35602-69-8 胆甾醇硬脂酸酯 | CAS号593-45-3 正十八烷 | CAS号34557-54-5 methane | CAS号629-78-7 正十七烷 | CAS号201230-82-2 carbon monoxide | CAS号1560-92-5 2-甲基二六烷 | CAS号1560-89-0 2-甲基十七烷

油酸甲酯置于grubbs Catalyst First Generation,Potassium Tert-Butylate,氢气体系中,用 四氢呋喃 用作溶剂,70.0 °C,5.0 Mpa 条件下,反应 16.0H,反应生成硬酯酸甲酯c18
参考文献:通过串联烯烃复分解-酯加氢从可再生脂肪酸中得到的长链[小α]-[小ω]二醇
标题:通过串联烯烃复分解-酯加氢从可再生脂肪酸中得到的长链[小α]-[小ω]二醇
摘要:按照正交串联的自复分解-酯氢化方案,很容易从可再生的脂肪酸甲酯中获得长链α-小ω二醇.
Doi:10.1039/c7Gc00192D

专利信息

专利号:US-8569560-B2
优先权日:2006-10-13
标题 :Synthesis of terminal alkenes from internal alkenes via olefin metathesis
发明人：SCHRODI YANN; PEDERSON RICHARD L; KAIDO HIROKI; TUPY MICHAEL J
权利人:ELEVANCE RENEWABLE SCIENCES
摘要:This disclosure relates generally to olefin metathesis, and more particularly relates to the synthesis of terminal alkenes from internal alkenes using a cross-metathesis reaction catalyzed by an olefin metathesis catalyst. According to one aspect, for example, a method is provided for synthesizing a terminal olefin, the method comprising contacting, in the presence of a ruthenium alkylidene metathesis catalyst, an olefinic substrate comprised of at least one internal olefin with a cross metathesis partner comprised of an alpha olefinic reactant, under reaction conditions effective to allow cross-metathesis to occur, wherein the reaction conditions include a reaction temperature of at least 35° C. The methods, compositions, reactions and reaction systems herein disclosed have utility in the fields of catalysis, organic synthesis, and industrial chemistry.

专利号:US-11680224-B2
优先权日:2020-11-04
标 题:Hydroxy fatty acid synthesis
发明人：CERMAK STEVEN C; Isbell Terry; LOWERY BENJAMIN A
权利人:US AGRICULTURE; THE US SECRATERY OF AGRICULTURE
摘要:The invention relates to methods for the synthesis of hydroxy fatty acids from unsaturated fatty acids via epoxidation and catalytic hydrogenation.

专利号:US-5872245-A
优先权日:1992-09-30
标题 :Continuous process for the synthesis of sucrose fatty acid esters
发明人：WILSON DONALD C
权利人:OPTIMA TECHNOLOGIES GROUP
摘要:This present invention pertains to a process for the synthesis of sucrose fatty acid esters by reacting sucrose and a purified specific fatty acid ester under substantially solvent free conditions in the presence of a transesterification stationary catalyst and mechanical emulsification. The process is continuous, yielding selected individual products of separated simple sucrose fatty acid esters of mono-, di-, tri- and polyesters while recycling the unwanted ester fractions, the unreacted sucrose and fatty acid ester.

专利号:US-8647848-B2
优先权日:2008-06-13
标题:Enzymatic synthesis of sphingolipids
发明人：HOLLMANN FRANK; THUM OLIVER; TOELLE CHRISTOPH; PROVINZANO ANGELO; KOREVAAR CORNELIS GERRIT NIJS
权利人:HOLLMANN FRANK; THUM OLIVER; TOELLE CHRISTOPH; PROVINZANO ANGELO; KOREVAAR CORNELIS GERRIT NIJS; EVONIK GOLDSCHMIDT GMBH
摘要:The invention relates to the enzymatic synthesis of sphingolipids and compositions that contain sphingolipids from lysosphingolipids and carbonic esters, and to cosmetic, dermatological or pharmaceutical formulations containing said sphingolipids or compositions.

专利号:US-5646319-A
优先权日:1995-06-23
标题:Synthesis of N-acyl-N-alkylcarboxylates
发明人：LETTON JAMES CAREY; MILLER LARRY EUGENE
权利人:PROCTER & GAMBLE
摘要:Chemical synthesis of N-acyl-N-alkylcarboxylates through oxidation of substituted amides formed from carboxylic acid esters and an N-alkyl-N-alkanolamine.

专利号:US-5338686-A
优先权日:1992-04-29
标 题:Method for measuring in vivo synthesis of biopolymers
发明人：HELLERSTEIN MARC K
权利人:HELLERSTEIN MARC K
摘要:A method for determining the mass isotope enrichment of a subunit from which a biopolymer is formed, and the rates of synthesis and decay of the biopolymer. The mass isotope enrichment of the subunit is determined by comparing the mass isotopomer distribution of the biopolymer after administration of a mass isotopically labeled subunit, with the expected frequencies of the different mass isotopomers produced from a given subunit mass isotope enrichment. To determine the synthesis rate of the biopolymer, the expected frequency of a selected biopolymer mass isotopomer, calculated from the subunit isotope enrichment, is compared with the actual frequency of that biopolymer mass isotopomer. To determine biopolymer decay, the decay rate of high mass isotopomers of the biopolymer is determined.