CAS: 2051-31-2; Decan-4-Ol

该化合物是一种直链脂肪酒精,由10碳链和氢氧(-OH)组组成,位于第四碳上;该化合物在室内温度下无色可粉黄黄色液体,具有典型的脂肪味;在水中略微溶解,但在乙醇和乙醇等有机溶剂中较易溶解;4-Decanol显示出典型的酒精特性,包括参与氢结合的能力,这导致氢的沸点相对高于类似分子重量的碳氢化合物;它被用于各种用途,包括表面活性剂,乳化剂和其他化学化合物的合成;此外,4-decanol还存在于某些自然来源中,有时用于香味和调味的配制;安全数据表明,应谨慎处理,因为接触时可能会引起皮肤和眼部的刺激.

结构式图片

相似化合物

593-03-3 624-08-8 23708-56-7

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

heptanal di-n-propyl zinc (S)-(E)-4-(dimethylphenylsilyl)-2-decene decane decan-4-one Toluene-4-sulfonic acid 1-propyl-heptyl ester 6-hexyltetrahydro-2H-pyran-2-one

合成工艺路线路线简述

    📜2-壬烯-1-醇置于nickel Diacetate Titanium(Iv) Isopropylate,叔丁基过氧化氢,锰,Sodium Tetrahydroborate,Copper(L) Iodide,L-(+)-酒石酸二乙酯,1,4-环己二烯,氢气,2,4,6-Collidine Hydrochloride,乙二胺体系中,用 四氢呋喃,甲醇,乙醚,二氯甲烷 用作溶剂,化学反应 10.17H,反应生成4-正癸醇
    参考文献:Titanocene-Catalyzed Regiodivergent Epoxide Openings
    标题:Titanocene-Catalyzed Regiodivergent Epoxide Openings
    摘要:The First Regiodivergent Opening Of Unbiased Epoxides Providing The Ring-Opened Products In High Enantiomeric Excess From Racemic And Exceptionally High Enantiomeric Excess From Enantioenriched Substrates In A Double Asymmetric Process Has Been Devised. It Constitutes A More General Case Of The Very Important Enantioselective Openings Of Meso-Epoxides.
    Doi:10.1021/ja0686211

    海关参考信息

    专利信息


    专利号:US-6384228-B2
    优先权日:1998-05-26
    标题 :Method for synthesis of halopyridyl-azacyclopentane derivative and intermediate thereof
    发明人:NODE MANABU; NAKAMURA DAISAKU; FUJIWARA TOSHIO; ICHIHASHI SHOGO
    权利人:NIHON MEDIPHYSICS CO LTD
    摘要:The present invention relates to a method for synthesis of an optically active halopyridyl-azacyclo-pentane derivative and the intermediate thereof which comprises preparing an optically active allene-1,3-dicarboxylic acid ester derivative from an optically active acetonedicarboxylic acid ester derivative and then proceeding through a 7-azabicyclo[2.2.1]heptane derivative to obtain the objective product.

    专利号:US-2009318592-A1
    优先权日:2005-10-11
    标 题 :Process for the Synthesis of Amine Ethers
    发明人:FREY MARKUS; BROENNIMANN VALERIE
    权利人:CIBA GEIGY CORP
    摘要:The present invention relates to novel processes for the preparation of a sterically hindered amine ether by reacting a corresponding sterically hindered amine oxide with a ketone or an aldehyde with at least one reactive H in the presence of a peroxydisulphate. Products obtained by this process may be hydrogenated. The compounds made by these processes are particularly effective in the stabilization of polymer compositions against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.

    专利号:US-2007191516-A1
    优先权日:2004-03-15
    标题 :Process for the synthesis of amine ethers
    发明人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
    权利人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
    摘要:A process for the preparation of a sterically hindered amine ether which comprises reacting a corresponding sterically hindered aminoxide with a C 5 -C 18 alk-1-ene in the presence of an organic hydroperoxide and optionally hydrogenating the resulting product as well as the product mixtures obtained therewith and their use as stabilizers and flame retardants.

    专利号:US-7342140-B2
    优先权日:2002-09-12
    标题:Method for the production of polyetherols
    发明人:BOHRES EDWARD; HIBST HARTMUT; STOESSER MICHAEL; RUPPEL RAIMUND; BAUM EVA
    权利人:BASF AG
    摘要:The present invention relates to a process for preparing a polyetherol which comprises reacting at least one alkylene oxide with at least one starter compound in the presence of a catalyst of the formula I:n nM 1 p [M 2 q O n (OH) 2(3-n) ] x ,  (I)n nand to the polyetherols prepared by such a process and to their use for the synthesis of polyurethanes, as fuel additive or as surfactant.

    专利号:US-7402675-B2
    优先权日:2000-05-26
    标题 :Process for the synthesis of amine ethers from secondary amino oxides
    发明人:HAFNER ANDREAS; KIRNER HANS JUERG; SCHWARZENBACH FRANZ; VAN DER SCHAAF PAUL ADRIAAN; NESVADBA PETER
    权利人:CIBA SC HOLDING AG
    摘要:An amine ether of formula A n nwherein a is 1 or 2; and when a is 1, E is E′; when a is 2, E is L;n E′ is C 1 -C 36 alkyl; C 3 -C 18 alkenyl; C 2 -C 18 alkinyl; C 5 -C 18 cycloalkyl; C 5 -C 18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or tricyclic hydrocarbon of 7 to 12 carbon atoms; C 2 -C 7 alkyl or C 3 -C 7 alkenyl substituted by halogen; C 7 -C 15 aralkyl or C 7 -C 15 aralkyl substituted by C 1 -C 4 alkyl or phenyl; or E′ is a radical of formula (VII) as explained in claim 1; T′ is tertiary C 4 -C 18 alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR 21 or C(O)—R 22 ; or T′ is C 5 -C 12 cycloalkyl; C 5 -C 12 cycloalkyl which is interrupted by at least one O or —NR 18 —; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or —NR 18 —; or T′ is —C(G 1 )(G 2 )-T″; or C 1 -C 18 alkyl or C 5 -C 12 cycloalkyl substituted by n n n n n n n n n n n n T″ is hydrogen, halogen, NO 2 , cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; n or T″ and T′ together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G 1 and G 2 , an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, n are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E 1 -H or H-L-H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. n n n n n The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.

    专利号:US-5637757-A
    优先权日:1995-04-11
    标 题 :One-pot synthesis of ring-brominated benzoate compounds
    发明人:HILL JOHN E; FAVSTRITSKY NICOLAI A; MAMUZIC RASTKO I; BHATTACHARYA BHABATOSH
    权利人:GREAT LAKES CHEMICAL CORP
    摘要:A method of preparing tetrabromobenzoate compounds from tetrabromophthalic anhydride by reacting tetrabromophthalic anhydride with alcohol in the presence of a decarboxylation catalyst. The reaction may be carried out in an excess of alcohol, or with a near stoichiometric amount of alcohol by performing the reaction in an inert solvent.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Aitken, R. A.; Boubalouta, Y., Science of Synthesis Knowledge Updates, (2013) 4, 137.
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