CAS: 693-54-9; Decan-2-One

该化合物是具有分子式C10H20O的饱和性脂酮,其特征为清晰,无色外观和独特的水果味,通常用作有机合成的中间体,并因其在标准条件下的有利化学稳定性和低反应性而用作调味剂.Decan-2-1在有机溶剂中表现出中等溶性,水溶性有限,适合在香料,药品和特殊化学品中应用.其明确界定的结构和可预测的再活性有助于其在受控合成工艺中的用途.

结构式图片

相似化合物

33758-15-5 111-13-7 112-12-9

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号872-05-9 正癸烯 | CAS号764-93-2 1-癸炔 | CAS号1120-06-5 2-癸醇 | CAS号31637-05-5 2-methyl-2-°Cty... | CAS号3695-29-2 5-iodopentan-2-one | CAS号6393-56-2 正戊基氯化镁 | CAS号122-39-4 二苯胺 | CAS号111-66-0 1-辛烯 | CAS号106094-59-1 N-[(Z)-decan-2-... | CAS号21078-68-2 3-Undecanol, 3-... | CAS号105-21-5 丙位庚内酯 | CAS号104-50-7 丙位辛内酯 | CAS号3128-06-1 5-氧代己酸 | CAS号123-76-2 乙酰丙酸 | CAS号3128-07-2 5-乙酰戊酸 | CAS号1117-74-4 4-氧代-己酸 | CAS号111-66-0 1-辛烯 | CAS号824-58-8 Ethanone, 1-bic...

合成工艺路线路线简述

  • 合成目标产物 2-Decanone 主要起始原料 1-Decene
  • (文献来源)合成步骤主要原料 1-Decene
十一碳-2-炔酸置于air,[au(Dpb)Sbf6]2(Cod)体系中,用 1,2-二氯乙烷 作为反应溶剂,化学反应 24.0H,反应生成 2-癸酮
参考文献:具有 L2/z 型二膦硼烷配体的炔衍生物的金催化形式水合,脱羧和 [4+2] 环加成
标题:具有 L2/z 型二膦硼烷配体的炔衍生物的金催化形式水合,脱羧和 [4+2] 环加成
摘要:使用以 Z 配体为特征的 Au 催化剂开发了炔烃的催化形式水合和炔酸的脱羧.此外,Al的分子内[4+2]环加成...
DOI:10.1246/cl.180610

海关参考信息

专利信息


专利号:WO-2008115912-A1
优先权日:2007-03-21
标题:Regio-specific synthesis of 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylic acid
发明人:KUBIAK GREGORY G; LYTHGOE DAVID J; YU YONG
权利人:SANOFI AVENTIS; KUBIAK GREGORY G; LYTHGOE DAVID J; YU YONG
摘要:This invention is directed to a five step regio-specific synthesis of 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylic acid compound of formula 16 comprising the steps of acetalating 3-methyl-thiophene-2-carbaldehyde in an alcohol solvent; iodinating the acetalated 3-methyl-thiophene-2-carbaldehyde in an non-protic polar or hydrocarbon solvent to yield the corresponding iodinated and acetalated 3-methyl-thiophene-2-carbaldehyde product; treating the iodinated and acetalated product with water to yield the corresponding 5-iodo-3-methyl-thiophene-2-carbaldehyde; oxidizing the 5-iodo-3-methyl-thiophene-2-carbaldehyde to the corresponding 5-iodo-3-methyl-thiophene-2-carboxylic acid in ketone solvent; Ullmann coupling of the 5-iodo-3-methyl-thiophene-2-carboxylic acid with alkali metal propoxide salt using a copper catalyst in propanol to yield 3-methyl-5-propoxy-thiophene-2-carboxylic acid; esterifying 3-methyl-5-propoxy-thiophene-2-carboxylic acid to yield the corresponding alkyl 3-methyl-5-propoxy-thiophene-2-carboxylate; brominating the 3-methyl-5-propoxy-thiophene-2-carboxylic acid to yield the corresponding alkyl 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylate; and basic hydrolyzing the alkyl 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylate with base to yield 4-bromo-3-methyl-5-propoxy-thiophene-2-carboxylic acid.

专利号:US-9085538-B2
优先权日:2010-07-26
标题:Process for the preparation of key intermediates for the synthesis of statins or pharmaceutically acceptable salts thereof
发明人:CASAR ZDENKO; STERK DAMJAN; JUKIC MARKO
权利人:CASAR ZDENKO; STERK DAMJAN; JUKIC MARKO; LEK PHARMACEUTICALS
摘要:The invention relates to commercially viable process for the synthesis of key intermediates for the preparation of statins, in particular Rosuvastatin and Pitavastatin or respective pharmaceutically acceptable salts thereof. A new simple and short synthetic route for key intermediates is presented which benefits from the use of cheap and readily available starting materials, by which the conventionally most frequently used DIBAL-H as reducing agent can be avoided.

专利号:US-10040752-B2
优先权日:2015-08-24
标 题 :Synthesis of levomethadone hydrochloride or dextromethadone hydrochloride and methods for use thereof
发明人:MKRTCHYAN GNEL; YAO QINGWEI
权利人:CODY LABORATORIES INC
摘要:Highly efficient methods for synthesis of levomethadone hydrochloride or dextromethadone hydrochloride are provided starting from D-alanine, or L-alanine, respectively, with retention of configuration. Methods for treating a subject are provided comprising administering a composition comprising an effective amount of levomethadone hydrochloride having not more than 10 ppm dextromethadone.

专利号:EP-2173747-B1
优先权日:2007-06-26
标 题:A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; R KYEN OMAR; URMANN MATHIAS; HALLAND NIS
权利人:SANOFI SA
摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R1; R2; R3; R4; J1; J2; J3; J4 and G have the meanings indicated in the claims. The present invention provides a direct metal, e.g. palladium or copper, catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

专利号:US-5681978-A
优先权日:1993-07-07
标题:Method for the stereocontrolled synthesis of stegobinone and useful borane intermediates
发明人:MATTESON DONALD S; MAN HON-WAH; HO OLIVER
权利人:UNIV WASHINGTON
摘要:A method of synthesis of (2S,3R,1'R)-stegobinone(I) using borane intermediates and methods for the use of stegobinone (I) for attracting beetles of the Anobium species.

专利号:US-9096519-B2
优先权日:2013-01-10
标 题 :Process for the synthesis of ketones from internal alkenes
发明人:MORANDI BILL; GRUBBS ROBERT H; WICKENS ZACHARY K; LERCH MICHAEL M
权利人:CALIFORNIA INST OF TECHN
摘要:The present invention is directed to methods for oxidizing internal olefins to ketones. In various embodiments, each method comprising contacting an organic substrate, having an initial internal olefin, with a mixture of (a) a biscationic palladium salt; and (b) an oxidizing agent; dissolved or dispersed in a solvent system to form a reaction mixture, said solvent system comprising at least one C 2-6 carbon nitrile and optionally at least one secondary alkyl amide, said method conducted under conditions sufficient to convert at least 50 mol % of the initial internal olefin to a ketone, said ketone positioned on a carbon of the initial internal olefin. The transformation occurs at room temperature and shows wide substrate scope. Applications to the oxidation of seed oil derivatives and a bioactive natural product are described.
杭州凯邦生物科技有限公司
⚠️ 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.chemspon.com
企业联系电话:0571-88937695👤
📞杭州凯邦生物科技有限公司 ⚠️参考联系方式
联系人:项经理
电话:0571-88937695
手机:13606537248
传真:0571-88933015
邮箱:sales@chemspon.com
通信地址: 浙江省杭州市拱墅区祥园路39号
邮编: 310015
🆔 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:浙江省杭州市拱墅区祥园路39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
现货

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

[参考文献]: Brian D Fitz, Et Al. Evaluation Of Injection Methods For Fast, High Peak Capacity Separations With Low Thermal Mass Gas Chromatography. J Chromatogr A. 2015 May 1:1392:82-90.
[参考文献]: H F Chen, Et Al. Ketone Ec50 Values In The Microtox Test. Ecotoxicol Environ Saf. 1995 Mar;30(2):120-3.
[参考文献]: Hyun Jin Lee, Et Al. Brushed Block Copolymer Micelles With Ph-Sensitive Pendant Groups For Controlled Drug Delivery. Pharm Res. 2013 Aug;30(8):2077-86.
[参考文献]: Pascal Fuchsmann, Et Al. Olfactometry Profiles And Quantitation Of Volatile Sulfur Compounds Of Swiss Tilsit Cheeses. J Agric Food Chem. 2015 Sep 2;63(34):7511-21.
[参考文献]: Peter S Toth, Et Al. Novel Organic Solvents For Electrochemistry At The Liquid/liquid Interface. Analyst. 2015 Mar 21;140(6):1947-54.

合成参考文献


摘要:Matsunaga, S., Science of Synthesis Knowledge Updates, (2010) 4, 219.
摘要:Santana, V. C. S.; Munaretto, L. S.; de Lucca, E. C., Jr., Science of Synthesis Knowledge Updates, (2022) 1, 173.
摘要:Croft, R. A.; Bull, J. A., Science of Synthesis Knowledge Updates, (2018) 4, 386.
摘要:De Wildeman, S.; Sereinig, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 169.
摘要:Aggarwal, V. K.; McGarrigle, E. M.; Shaw, M. A., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 313.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知