CAS: 1444-65-1; 2-Phenylcyclohexanone

该化合物是一种有机化合物,其特征是环己酮环在2位置被一个苯基组所取代,是一种氯酮,这意味着其结构内含有碳基组(C=O),该化合物一般是一种无色的,具有独特芳香味的浅黄色液体,在乙醇和乙醚等有机溶剂中具有中溶性,但由于其水分恐惧环,其溶解性在水中有限.该苯基组的存在有助于其稳定性和影响其再活动,使其在各种化学合成和应用中有用,包括作为有机合成中的中间体和生产红芳香.2-苯环己酮可进行典型的氯酮反应,例如核激素添加和氧化.在处理该化合物时,应采取安全防范措施,因为若吸入或浸入,可能会对健康造成危害,并应使用适当的防护设备.

结构式图片

相似化合物

2362-61-0 34281-92-0 1444-64-0

上下游产品

CAS号2362-61-0 反-2-苯基-1-环己醇 | CAS号108-94-1 环己酮 | CAS号108-90-7 氯苯 | CAS号108-86-1 溴苯 | CAS号64020-33-3 1-phenylhex-5-e... | CAS号100-59-4 苯基氯化镁 | CAS号771-98-2 1-苯基-1-环己烯 | CAS号822-87-7 2-氯环己酮 | CAS号98-80-6 苯硼酸 | CAS号1444-64-0 2-苯基环己醇 | CAS号105593-82-6 1-(2-methylsela... | CAS号4144-62-1 5-苯甲酰基戊酸 | CAS号65-85-0 苯甲酸 | CAS号4248-25-3 ethyl 6-oxo-6-p... | CAS号22591-17-9 (NZ)-N-(2-pheny... | CAS号2201-17-4 N,N-二甲基-1-苯基环己烷-1-胺 | CAS号771-98-2 1-苯基-1-环己烯 | CAS号98919-68-7 (1R,2S)-反-2-苯基-1-环己醇 | CAS号34281-92-0 (1S,2R)-反-2-苯基-1-环己醇 | CAS号827-52-1 环己基苯

合成工艺路线路线简述

  • 合成目标产物 2-Phenylcyclohexanone 主要起始原料 Cyclohexanone And Chlorobenzene
  • (文献来源)合成步骤主要原料 Cyclohexanone 和 Chlorobenzene
1-(4-喹啉基)甲胺置于甲醇,Sodium Tetrahydroborate,四(三苯基膦)钯,Cerium(III) Chloride Heptahydrate,15% Palladium On Carbon,氢气,Potassium Carbonate,溶剂黄146,1,1'-(Phenyl-λ3-Iodane)Bis(Pyridinium) Trifluoromethanesulfonate体系中,用 甲醇,1,2-二氯乙烷,甲苯 用作溶剂,化学反应 25.0H,反应生成2-苯基环己酮
参考文献:N-连接的λ3-碘化物对赤道醇的化学选择性氧化
标题:N-连接的λ3-碘化物对赤道醇的化学选择性氧化
摘要:复杂多元醇中醇的位点选择性和化学选择性官能化仍然是一个艰巨的合成挑战.尽管在氧中心的选择性衍生化方面已取得重大进展,但化学选择性氧化为相应的羰基的进展却很少.在循环系统中,虽然对轴型醇的选择性氧化是众所周知的,但尚未报道互补的赤道选择性过程.本文中,我们报道了氮连接的(双)阳离子λ3-碘(n-Hvis)在醇氧化中的应用以及它们对赤道醇与轴向醇的氧化选择性的空前水平.条件温和,简单的吡啶连接试剂(py-Hvi)可以很容易地从商业phi(oac)2合成,可以分离或原位生成.
Doi:10.1021/acs.Orglett.9B02018

海关参考信息

专利信息


专利号:US-4895996-A
优先权日:1988-10-17
标 题 :Synthesis of alkenes from enamines via hydroboration
发明人:GORALSKI CHRISTIAN T; SINGARAM BAKTHAN; BROWN HERBERT C
权利人:PURDUE RESEARCH FOUNDATION; DOW CHEMICAL CO
摘要:Alkenes are prepared by the hydroboration of enamines followed by an elimination reaction to form the alkene. This process has wide applicability and is useful for the stereospecific synthesis of [Z] isomers. It is preferred to use 9-borabicyclo[3.3.1 nonane as the hydroborating agent and to use methanol to catalyze the elimination reaction.

专利号:US-7884243-B2
优先权日:2003-12-22
标 题:Process for the synthesis of eneamide derivatives
发明人:BURGOS ALAIN; BERTRAND BLANDINE; ROUSSIASSE SONIA; PLUVIE JEAN-FRANCOIS; BLANCHET SYLVIE; MARTIN JULIETTE; PERRIN FLORENCE; BOURDEAU FRANCOISE
权利人:ZACH SYSTEM
摘要:A process for the production of ene-amide derivatives represented by the formula (I) n nwherein R1 and R2 and R3 are independently a hydrogen atom, an alkyl, a cycloalkyl, a cycloalkylalkyl, an alkylaryl, an aryl, a heterocycle, a cyano, an alkoxy, an aryloxy, a carboxyl, a carbamoyl, —CONR5R6 (in which R5 and R6 are independently an alkyl, arylalkyl or aryl group said ring being substituted or not with a functional group or with R5) or —COOR5 group (in which R5 is an alkyl, alkylaryl or aryl group), said alkyl, cycloalkyl, cycloalkylalkyl, alkylaryl and aryl groups being substituted or not with a functional group or with R5; or R1 and R2 taken together, may form a ring (which terms includes mono-, di- and higher polycyclic ring systems); R4 is a hydrogen atom, an alkyl, an aryl, an alkylaryl, said groups are substituted or not with a halogen atom as Cl, Br, or F; X is an oxygen atom or a leaving group and m is an integer 1 or 2; when m is 1 then X is a leaving group; when m is 2 then X is a oxygen atom, which comprise: a hydrogenation/isomerization reaction in presence of a heterogeneous catalyst, of an oxime derivatives of formula (II)n n nwherein R1, R2 and R3 are as defined above with an acyl derivative of formula (III) (R4CO) m X wherein R4, m and X are as defined above.

专利号:US-3814767-A
优先权日:1972-04-07
标 题 :Process for preparing bicyclo alkyl derivatives
发明人:WARD F
权利人:MILES LAB
摘要:A PROCESS FOR THE SYNTHESIS OF BICYCLO ALKYL DERIVATIVES OF THE STRUCTUAL FORMULA: 2,6-(-CH2-X-CH2-),2-R4,3-R1,4-R2,5-R5-CYCLOHEXANONE IN WICH R1 IS H OR PHENYL, R2 IS H OR ALKYL, R4 IS H PHENYL OR SUBSTITUTED PHENYL IN WHICH THE SUBSTITUENTS ARE HALOGEN, ALKOXY, OR ALKYL, R5 IS 4-(R3-PHENYL)PIPERAZINO OR 4-(R3-PHENYL)PIPERIDINO, R3 IS H, HALOGEN, ALKOXY OR CF3, AND X IS A POLYCARBON LOWER ALKYLENE RADICAL OF BETWEEN 0 AND 2 CARBON ATOMS INCLUSIVE, COMPRISING THE FOLLOWING REACTION SEQUENCE: O=CH-CH(-R2)-CH(-R1)-C(-R4)<(-CO-CH2-CH2-X-CH2-) + H-R5 --> (- H2O) R5-CH=C(-R2)-CH(-R1)-C(-R4)<(-CO-CH2-CH2-X- CH2-) --> (DELTA, DMF OR (I-PR-)OH, (ET-)3-N) 2,6-(-CH2-X- CH2-),2-R4,3-R1,4-R2,5-R5-CYCLOHEXANONE THE COMPOUNDS PREPARED ACCORDING TO THE PROCESS OF THIS INVENTION HAVE BENEFICIAL PHARMACOLOGICAL PROPERTIES.

专利号:CN-115161297-A
优先权日:2022-05-09
标 题 :Three-enzyme nanoreactor and its application and synthesis of chiral tertiary α-phenylcycloalcohol

专利号:US-7132092-B2
优先权日:2002-02-08
标 题:Metallized mesoporous silicate and method of oxidation with the same
发明人:HAGIYA KOJI
权利人:SUMITOMO CHEMICAL CO
摘要:A metallized mesoporous silicate which is obtained by (i) reacting (a) either a metal peroxide obtained by the reaction of an aqueous hydrogen peroxide solution with at least one metal or metal compound selected from the group consisting of the following 1) to 4) 1) tungsten 2) molybdenum 3) vanadium 4) compounds comprising 4 a ) any of tungsten, molybdenum, and vanadium and 4 b ) at least one element selected from Groups 13 to 16 (excluding oxygen) or a solution of the metal peroxide with (b) a silicon compound in the presence of an alkylamine or a quaternary ammonium salt and separating the resultant silicate; and a process for producing the metallized mesoporous silicate. Also provided is a method of organic synthesis with the silicate.

专利号:US-2007129573-A1
优先权日:2003-12-22
标 题:Process for the synthesis of eneamide derivatives
武汉市罗氏科技发展有限公司
⚠️ 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.luoshikg.com
企业联系电话:18986168071;19307247857👤
📞武汉市罗氏科技发展有限公司 ⚠️参考联系方式
联系人:罗经理;祝经理
电话:18986168071;19307247857
手机:18986168071;19307247857
传真:027-88121016;QQ1712680783
邮箱:18986168071@163.com
通信地址: 湖北省武汉市洪山区洪山工业园
邮编: 430064
🆔 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:湖北省武汉市洪山区洪山工业园
⚠️ 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。
杭州科耀医药科技有限公司
⚠️ 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.searchem.net
企业联系电话:0571-58120272;17185714011;13067805092👤
📞杭州科耀医药科技有限公司 ⚠️参考联系方式
联系人:黄经理
电话:0571-58120272;17185714011;13067805092
手机:17185714011;13067805092
传真:0571-58120272
邮箱:sales@search.com
通信地址: 杭州下沙21号大街600号海创园5号楼四楼(西)
邮编: 310000
🆔 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:杭州下沙21号大街600号海创园5号楼四楼(西)
⚠️ 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

合成参考文献


摘要:Hari, Y.; Aoyama, T.; Shioiri, T., Science of Synthesis Knowledge Updates, (2010) 4, 60.
摘要:Li, W.; Liu, X. H.; Feng, X. M., Science of Synthesis Knowledge Updates, (2021) 1, 54.
摘要:Jie, X.; Su, W., Science of Synthesis, (2022) , 2.
摘要:Arai, N.; Ohkuma, T., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 30.
摘要:de Gonzalo, G.; van Berkel, W. J. H.; Fraaije, M. W., Science of Synthesis: Biocatalysis in Organic Synthesis, (2015) 3, 214.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知