CAS: 13019-22-2; 9-Decen-1-Ol

该化合物是一种不饱和的脂肪酒精,其特征为长碳链,具有氢氧基组第九碳的双重结合,其分子式为C10H20O,表明其含有10个碳原子,20个氢原子和1个氧原子.该化合物一般是无色的,可粉黄,具有典型脂肪味,在有机溶剂中可溶解,但由于其疏水性碳链,其溶解性在水中有限.9-Decen-1-ol因其在香味和口味工业中的应用以及表面活性剂和乳化剂的生产中的应用而闻名.此外,它可以作为有机合成的前体,特别是在形成其他化学化合物时.存在双重结合有助于其再活性,允许其参与各种化学反应,包括氧化和聚合.应当参考安全数据,以便处理和接触准则,以及任何化学物质.

结构式图片

相似化合物

25601-41-6 14436-32-9 112-43-6

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

CAS号25601-41-6 9-Dec烯酸甲酯 | CAS号67233-91-4 ethyl 9-decenoate | CAS号112-47-0 1,10-癸二醇 | CAS号67136-13-4 2-dec-9-enoxyoxane | CAS号39770-05-3 9-癸烯醛 | CAS号100189-71-7 dec-9-enoxymeth... | CAS号53463-68-6 10-溴-1-癸醇 | CAS号3669-80-5 11-羟基十一烷酸 | CAS号1647-16-1 1,9-癸二烯 | CAS号14436-32-9 9-癸烯酸 | CAS号3788-56-5 9-羟基壬酸 | CAS号56683-54-6 顺式-11-十六烯-1-醇 | CAS号50816-18-7 乙酸-9-癸烯基酯 | CAS号142580-79-8 ethyl 4-dec-9-e... | CAS号91717-85-0 1,2,10-癸三醇 | CAS号53463-68-6 10-溴-1-癸醇 | CAS号1275582-65-4 9-bromodecanol | CAS号127102-48-1 1,2-Epoxydecan-10-ol | CAS号17643-36-6 9-癸炔-1-醇 | CAS号19754-58-6 10-(Tetrahydro-...

合成工艺路线路线简述

  • 合成目标产物 9-Decen-1-Ol 主要起始原料 1,10-Decanediol
  • (文献来源)合成步骤主要原料 1,10-Decanediol
1,10-癸二醇置于potassium Tert-Butylate,四丁基溴化铵,氢溴酸体系中,用 四氢呋喃,水,甲苯 用作溶剂,化学反应 0.58H,反应生成9-十烯-1-醇
参考文献:艾地苯醌新工艺的合成路线发现和引进优化
标题:艾地苯醌新工艺的合成路线发现和引进优化
摘要:公开了导致艾地苯醌的对环境无害,方便,高产率和成本有效的合成.该合成包括用于制备2-溴-3,4,5-三甲氧基-1-甲基苯的溴化工艺,使用热加热或微波加热进行的heck交叉偶联反应的方案,通过钯催化的氢化作用进行烯烃还原以及以过氧化氢为氧化剂的绿色氧化方案,以实现苯醌构架.总合成由六个步骤组成,可提供20%的总产率,相当于76%的步骤产率.
Doi:10.1021/op200051V

海关参考信息

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-6215019-B1
优先权日:1998-09-01
标题 :Synthesis of 5-decenyl acetate and other pheromone components
发明人:PEDERSON RICHARD L; GRUBBS ROBERT H
权利人:TILLIECHEM INC
摘要:The present invention relates to syntheses of 5-decenyl acetate, the major component in Peach Twig Borer pheromone, and other pheromone components. The syntheses entails few reaction steps, use commercially available starting materials, and have relatively short process times. A preferred embodiment of the syntheses involves self-metathesizing 1-hexene in the presence of Grubbs' catalyst, [(PCy3)2Cl2]Ru=CHPh. The resulting 5-decene is then reacted with an alcohol or acetate protected hexene under vacuum to yield 5-decenyl acetate. These syntheses produce good yields without the need for expensive or sophisticated equipment.

专利号:US-7901915-B2
优先权日:2005-09-19
标 题:Biocatalytic manufacturing of (meth) acrylic esters
发明人:SYMES KENNETH CHARLES; COLLIER SIMON ANDREW; ARMITAGE YVONNE CHRISTINE; MISTRY RAJESH; BARANYAI ROBERT
权利人:BASF SE
摘要:The invention relates to a biocatalytic method or process for the synthesis of esters of acrylic acid and/or methacrylic acid free of positively chargeable/charged groups, comprising reacting one or more alcohols (alcohol starting materials) which are free of positively chargeable or charged groups with (meth)acrylyl-CoA, preferably in the presence of a catalyst (inorganic, organic or organometallic, or preferably a biocatalyst) capable of effecting the transfer of an alcohol radical from an alcohol starting material as defined above or below to (meth)acrylyl CoA under removal of the CoA moiety transferase activity, such as an enzyme of the transferase or hydrolase class of enzymes. The (meth)acrylyl-CoA is preferably formed by reaction of (meth)acrylic acid or its salts with coenzyme A in the presence of an energy providing substance and a biocatalyst e.g. with S-acetyl coenzyme A synthetase activity or by reaction of acrylate or methacrylate produced metabolically in the presence of a biocatalyst or metabolically.

专利号:US-12344573-B2
优先权日:2018-07-16
标题:Synthesis of straight-chain lepidopteran pheromones through one- or two-carbon homologation of fatty alkenes
发明人:WAMPLER KEITH M; LEE CHOON WOO; ROZZELL DAVID
权利人:PROVIVI INC
摘要:Methods for the preparation of alkenes including insect pheromones are described. The methods include homologation reactions employing reagents such as 1,3-diesters, epoxides, cyanoacetates, and cyanide salts for elongation of starting materials and intermediates by one or two carbon atoms. The alkenes include insect pheromones useful in a number of agricultural applications.

专利号:US-5753726-A
优先权日:1995-12-20
标 题:Synthesis of modified epoxy resins for cathodic electrodeposition with catalyst deactivation and diol modification
发明人:REUTER HARDY; JOUCK WALTER; OTT GUENTHER
权利人:BASF LACKE & FARBEN
摘要:Epoxy resins for preparing water-dispersible binders for cathodic electrodeposition coating materials, the epoxy resin being preparable by reacting a) polyepoxides having at least one glycidyl group per molecule b) and, optionally, up to 60% by weight, based on the overall epoxy resin reaction product, of aliphatic and/or alicyclic hydroxy compounds having preferably two or on average less than two hydroxyl groups per molecule and a molecular weight of less than 9000 g/mol, c) in the presence of a catalyst consisting of neutral metal salts, such as alkali metal salts and alkaline earth metal salts, zinc salts and nickel salts of tetrafluoroboric, tetrachloroboric, hexafluoro- antimonic,hexachloroantimonic,hexafluorophosphoric, perchlorate and periodic acid, and d) adding a deactivating agent which prevents the epoxy groups reacting further or effectively reduces the rate of such reaction as soon as the phenolic hydroxyl groups have already substantially reacted and at least 0.6% by weight of epoxy groups are still present, based on the overall weight of the epoxy resin reaction product.\\!

专利号:US-4935503-A
优先权日:1988-05-05
标题:Azidochlorination and diazidization of glycals
发明人:NAICKER SELVARAJ; NOUJAIM ANTHONY A
权利人:BIOMIRA INC
摘要:The invention describes a one-pot single step procedure for the azidochlorination or diazidization of glycals, including glycal elements of carbohydrates. Compounds such as 3,4,6-tri-O-benzyl-2-azido-2-deoxy-alpha-D-galactopyranosy chloride, and 3,4,6-tri-O-benzyl-2-azido-2-deoxy-alpha-,beta-D-galactopyranose are prepared from tri-O-benzyl galactal as well as 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-alpha-galactopyranasol chloride and 3,6-di-O-acetyl-4-O-[2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyl]-2-azido-2-deoxy-alpha-D-glycopyranosyl chloride from their respective O-acetylated glycal derivatives by the addition of azido chloride which is chemically generated in situ. A method using 3,4,6-tri-O-acetyl-2-azido-2-deoxy-alpha-D-galactopyranosyl chloride for the synthesis of antigenic determinants such as the terminal asialo GM 1 (beta-D-Gal (1->3)-beta-D-GalNAc-OR) has been demonstrated. The conversion of the subject synthon into 3,4,6-tri-O-acetyl-2-azido-2-deoxy-alpha-D-galactopyranosyl bromide and 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-alpha-D-galactopyranose is also described. A further method for the synthetic generation of the Tn antigen (alpha-D-GalNAc-O-L-serine) is also described.
铜陵立事达化学科技有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.lishidachem.cn
企业联系电话:18606623089;19064063435👤
📞铜陵立事达化学科技有限公司 ⚠️参考联系方式
联系人:瞿先生;刘经理
电话:18606623089;19064063435
手机:18606623089;19064063435

邮箱:350737036@qq.com
通信地址: 安徽省铜陵市郊区陈瑶湖镇其凤村向东路192号
邮编: 244061
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:安徽省铜陵市郊区陈瑶湖镇其凤村向东路192号
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Orthocarbonsäure-Ester Mit 2,4,10-Trioxaadamantanstruktur Als Carboxylschutzgruppe; Verwendung Zur Synthese Von Substituierten Carbonsäuren Mit Hilfe VonGrignard-Reagenzien
作者:Gundula Voss,Hans Gerlach |发布日期:1983.11.2
摘要:Ortho Esters With 2,4,10-Trioxaadamantane Structure As Carboxyl Protecting Group; Applications In The Synthesis Of Substituted Carboxylic Acids By Means Of Grignard Reagents

合成参考文献


摘要:Haufe, G., Science of Synthesis Knowledge Updates, (2019) 3, 208.
摘要:Haufe, G., Science of Synthesis Knowledge Updates, (2019) 3, 168.
摘要:Haufe, G., Science of Synthesis Knowledge Updates, (2019) 3, 225.
摘要:Wang, X.-Y.; Sun, X.-L., Science of Synthesis Knowledge Updates, (2020) 2, 453.
摘要:Pajkert, R.; Röschenthaler, G.-V., Science of Synthesis Knowledge Updates, (2022) 1, 402.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知