CAS: 1193-81-3; 1-Cyclohexylethanol

该化合物是一种有机化合物,其特点是存在环己醇组和乙醇杂质.该化合物的特征是乙醇组附属的环环,使它成为次要酒精.它一般是一种无色的淡黄色液体,具有一种特异的气味.分子结构有助于水中的中溶解性,而由于水分疏漏环己醇组,它更溶于有机溶剂. 1-Cyclohexyl乙醇展示酒精的典型特性,如形成氢结的能力,影响其沸点和粘度.它被用于各种用途,包括溶剂和其他有机化合物的合成.此外,它由于其香味,有可能在香味的香气中用于香味工业.应该参考安全数据,以便处理和接触任何化学物质,例如处理和接触准则.

结构式图片

相似化合物

3113-98-2 3113-99-3 823-76-7

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98-86-2 苯乙酮 | CAS号119-61-9 二苯甲酮 | CAS号823-76-7 乙酰基环己烷 | CAS号50-00-0 甲醛 | CAS号110-83-8 环己烯 | CAS号98-85-1 苏合香醇 | CAS号75-24-1 三甲基铝 | CAS号2043-61-0 环己烷甲醛 | CAS号695-12-5 乙烯基环己烷 | CAS号43125-06-0 1-cyclohexyl-3-... | CAS号823-76-7 乙酰基环己烷 | CAS号3113-98-2 (S)-1-cyclohexy... | CAS号3113-99-3 (R)-1-环己基-1-醇 | CAS号140390-59-6 1-cyclohexyleth... | CAS号67-63-0 异丙醇 | CAS号932-66-1 1-乙酰基-1-环己烯 | CAS号27607-65-4 1,3-dicyclohexy... | CAS号86728-93-0 甲基 (S)-4-氯-3-羟基丁酸酯

合成工艺路线路线简述

    苯乙酮置于氢气体系中,用 水 用作溶剂,20.0 °C,2.0 Mpa 条件下,反应 6.0H,以100%的收率获得1-环己基乙醇
    参考文献:用手性氨基酸接枝的β-环糊精:用于不对称氢化的纳米粒子的有希望的超分子稳定剂吗
    标题:用手性氨基酸接枝的β-环糊精:用于不对称氢化的纳米粒子的有希望的超分子稳定剂吗
    摘要:通过以下两种方法在水溶液中制备了嫁接有手性氨基酸部分(如1-丙氨酸(ala)和1-亮氨酸(leu))的随机甲基化β-环糊精(ramecd)稳定的水溶性钌纳米颗粒.适当的环糊精存在下一步法还原三氯化钌作为金属源的氢(一锅法)或(II)nabh 4还原金属盐,然后通过添加手性修饰的ramecd(级联法)来稳定钌水溶胶.通过tem和NMR分析研究了配体的性质和合成方法对所得钌胶体的尺寸,分散性和表面性质的影响.球形钌悬浮液包含非常小的粒径分布(0.82-1.00 Nm)的微粒.在各种手性化合物(烯烃,酮和双取代的芳烃)的双相加氢中评估了它们的催化性能,在活性和选择性方面均显示出令人鼓舞的结果.然而,没有观测到明显的对映体过量.
    Doi:10.1016/j.Apcata.2013.08.011

    海关参考信息

    专利信息


    专利号:US-6951932-B2
    优先权日:2001-10-25
    标 题:Synthesis of 2-aralkoxyadenosines and 2-alkoxyadenosines
    发明人:MOORMAN ALLAN R
    权利人:KING PHARMACEUTICALS RES & DEV
    摘要:The invention provides new methods for synthesis of 2-aralkyloxyadenosines and 2-alkoxyadenosines. The invention is particularly useful for synthesis of 2-[2-(4-chlorophenyl)ethoxy]adenosine. Preferred methods of the invention include activating a guanosine compound followed by hydrolysis; alkylating the hydrolyzed compound with subsequent animation to provide a 2-aralkyloxyadenosine or a 2-alkoxyadenosine compound.

    专利号:US-9365607-B1
    优先权日:2012-07-31
    标题 :Synthesis of deuterated ribo nucleosides, N-protected phosphoramidites, and oligonucleotides
    发明人:SRIVASTAVA SURESH C; YASKO AMY
    权利人:ASED LLC
    摘要:The present invention is directed towards the synthesis of high purity deuterated sugars, deuterated phosphoramidites, deuterated nucleobases, deuterated nucleosides, deuterated oligonucleotides, and deuterated RNA's of defined sequences which can exhibit biochemically useful and biologically valuable properties, thus having potential for therapeutic uses.

    专利号:US-5041637-A
    优先权日:1988-07-12
    标题:Process for the synthesis of optically active aminoacids
    发明人:CANNATA VINCENZO; TAMERLANI GIANCARLO; CALZOLARI CLAUDIO
    权利人:PRESIDENZA DEL CONSIGLIO DEL M
    摘要:New process for the synthesis of optically active aminoacids of formula ##STR1## by treating compounds of formula ##STR2## which an optically active alcohol of formula n n R.sub.4 --OH (III) n n n d or 1 n n To obtain a pair of diastereoiosmer esters of formula ##STR3## which is resolved in basic medium into the single diastereoisomer esters of formula ##STR4## from which the desired optically active aminoacid of formula (I) is obtained by treatment in acid medium.

    专利号:US-7342003-B2
    优先权日:2001-10-25
    标 题 :Synthesis of 2-aralkyloxyadenosines, 2-alkoxyadenosines, and their analogs
    发明人:MOORMAN ALLAN R; SCANNELL MICHAEL; BALASUBRAMANIAN THIAGARAJAN; OUTCALT RUSSELL; LEUNG EDWARD
    权利人:KING PHARMACEUTICALS RES & DEV
    摘要:Provided is a method for the synthesis of an aralkyloxyadenosine or an alkoxyadenosine. The method includes protecting the hydroxyl sugar groups with a protecting group to produce a protected halogenated adenosine. The protected halogenated adenosine is alkoxylated, and the hydroxyl sugar groups of the protected halogenated adenosine are deprotected to provide the aralkyloxyadenosine or alkoxyadenosine.

    专利号:US-8269047-B2
    优先权日:2009-07-23
    标题 :Synthesis of alpha-halo enones and enals
    发明人:ZHANG LIMING; YE LONGWU
    权利人:ZHANG LIMING; YE LONGWU; UNIV NEVADA
    摘要:A method for preparing an α-halo enal or enone from an unprotected propargyl alcohol and an electrophilic halogen source catalyzed by the combination of a gold catalyst complex and a metal co-catalyst complex is disclosed. The method can be further enhanced by addition of an additive that facilitates suppression of a des-halo derivative.

    专利号:US-6448425-B1
    优先权日:2002-02-19
    标题:Preparation of N-substituted aminoorganosilanes
    发明人:GEDON STEVEN C; HALE MELINDA
    权利人:CROMPTON CORP
    摘要:A process is disclosed for the synthesis of N-cycloalkylaminoalkylsilanes, wherein the process comprises hydrogenating the corresponding N-arylaminoalkylsilanes in the presence of a catalytically effective amount of a supported or unsupported catalyst selected from the group consisting of palladium, platinum, nickel, rhenium, rhodium, ruthenium, copper chromite, and mixtures of the foregoing.
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    合成参考文献


    摘要:Oishi, M.; Takikawa, H., Science of Synthesis Knowledge Updates, (2010) 4, 102.
    摘要:De Wildeman, S.; Sereinig, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 169.
    摘要:Zaidlewicz, M.; Pakulski, M. M., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 114.
    摘要:Stoltz, B.; Ebner, D. C.; Park, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 224.
    摘要:Arai, N.; Ohkuma, T., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 49.
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