CAS: 710-11-2; 2-Oxo-4-Phenylbutanoic Acid

该化合物是一种化学化合物,其结构特征包括一个苯环,附于甲型位置的丁亚酸和甲酮功能组,该化合物一般是白色至白晶状固体,在有机溶剂中可溶解,尽管其在水中的溶解性有限; 碳箱酸和甲酮功能组的存在有助于其再活动,使其能够参与各种化学反应,例如凝聚和酯化; 经常用于有机合成,并可作为生产药品或其他复杂有机分子的中间体; 此外,其独特的结构可影响其生物活动,使其对药用化学感兴趣; 处理和储存安全数据,如同任何化学物质一样,都应参考,以确保采取适当的防范措施.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号1327337-63-2 lithium 2-oxo-4... | CAS号64920-29-2 2-氧代-基丁酸乙酯 | CAS号125582-89-0 bis(prop-2-enyl... | CAS号17451-19-3 2-氧代-4-苯基-3-丁酸 | CAS号100-52-7 苯甲醛 | CAS号15814-45-6 allyl 3-phenylp... | CAS号83402-87-3 2-氧代-4-苯基丁酸甲酯 | CAS号7226-82-6 (RS)-2-hydroxy-... | CAS号103-63-9 β-溴苯乙烷 | CAS号943-73-7 L-高苯丙氨酸 | CAS号501-52-0 3-苯丙酸 | CAS号29678-81-7 (R)-2-羟基-4-苯丁酸 | CAS号115016-95-0 (S)-2-羟基-4-苯丁酸 | CAS号83402-87-3 2-氧代-4-苯基丁酸甲酯 | CAS号64920-29-2 2-氧代-基丁酸乙酯 | CAS号76547-98-3 赖诺普利 | CAS号85955-59-5 (R)-赖诺普利钠盐 | CAS号76420-72-9 依那普利拉 | CAS号1012-05-1 DL-高苯丙氨酸

合成工艺路线路线简述

    2-氧代-4-苯基丁酸甲酯置于氢氧化钾体系中,用 乙醇,水 作为反应溶剂,化学反应生成 2-氧代-4-苯基丁酸
    参考文献:Asymmetric Aerobic Oxidation Of α-Hydroxy Acid Derivatives By C4-Symmetric,Vanadate-Centered,Tetrakisvanadyl(V) Clusters Derived From N-Salicylidene-α-Aminocarboxylates
    标题:Asymmetric Aerobic Oxidation Of α-Hydroxy Acid Derivatives By C4-Symmetric,Vanadate-Centered,Tetrakisvanadyl(V) Clusters Derived From N-Salicylidene-α-Aminocarboxylates
    摘要:A Series Of Chiral Vanadyl(V) Methoxides Bearing 3-T-Butyl-5-Substituted N-Salicylene-L-Valinate And L-T-Leucinate As Chiral Auxiliaries Has Been Prepared. In All Cases Except The 3,5-Di-T-Butyl Analogue,They Exist As Monomers Both In Solution And In The Single Crystal State. In The Case Of The 3,5-Di-T-Butyl Analogue,The Architectural Nature Of The Vanadyl(V) Complex Highly Depends On The Base Used During The Complex Formation Event. A Pentanuclear C-4-Symmetric Complex Was Formed When Potassium Salts Were Employed Instead Of The Corresponding Sodium Salts. A Central Vanadate(V) Unit Serves To Grip Four Identical Chiral Monomeric Vanadyl(V) Units Together,By Which A Potassium Ion Sits On Top Of The Four Flanking Units Through Carbonyl Coordinations And Serves To Hold The Whole Cluster By Cooperation With The Central Vanadate(V) Unit. In Comparison With The Corresponding Monomeric Vanadyl(V) Methoxide Complex,The Cluster Complex Was Utilized To Facilitate The Asymmetric Aerobic Oxidations Of Various Racemic Alpha-Hydroxyesters,-Amides,And-Thioesters With Excellent Selectivity Factors (K(Rel) 40 To >500).
    DOI:10.1021/jo070575F

    海关参考信息

    专利信息


    专利号:WO-2023198025-A1
    优先权日:2022-04-11
    标题:Synthesis method and synthesis device for organic nitrogen-containing compound
    发明人:LI GUANGQIN; Liao Peisen; XIAN JIAHUI; LI SUISHENG; ZHANG YAWEI
    权利人:UNIV SUN YAT SEN
    摘要:The present invention relates to the field of organic synthesis, specifically to a synthesis method and synthesis device for an organic nitrogen-containing compound. Provided in the present invention is a synthesis method for an organic nitrogen-containing compound. In the method provided in the present invention, a porous carbon material is used as a catalyst, organic nitrogen-containing compounds such as an oxime, an amine, a nitrile and an amino acid are synthesized by means of an electro-catalysis method, byproducts are unlikely to generate, and the method is safe and environmentally friendly. Experiments show that organic nitrogen-containing compounds such as an amino acid, an oxime, an amine and a nitrile are successfully synthesized by using the method of the present invention, and the method has good Faraday efficiency and yield. In the present application, the synthesis of the above organic nitrogen-containing compounds can be realized by using nitrogen oxide waste gas or waste water as a raw material; and by converting the nitrogen oxide waste gas or waste water, the utilization of waste is realized, and the benefits are maximized. Further provided in the present invention is a synthesis device for an organic nitrogen-containing compound, which device is used for solving the defects of high energy consumption, long consumption time, and complex product separation and purification of existing synthesis methods.

    专利号:US-6033882-A
    优先权日:1994-07-07
    标题:Chiral synthesis of 2-hydroxy carboxylic acids with a dehydrogenase
    发明人:HOLBROOK JOSEPH JOHN; WILLIS CHRISTINE LOUISE; JOHNSEN KEYJI; HATELEY MARTIN JOHN
    权利人:GENZYME CORP
    摘要:PCT No. PCT/EP95/02692 Sec. 371 Date May 29, 1997 Sec. 102(e) Date May 29, 1997 PCT Filed Jul. 7, 1995 PCT Pub. No. WO96/01892 PCT Pub. Date Jan. 25, 1996Inter alia, an enzyme, a 2-hydroxy carboxylic acid dehydrogenase, characterised in that it is obtainable from Lactobacillus delbrueckii ssp. Bulgaricus and in that it catalyses the production of (R)-hydroxy derivatives of 2-keto acids, which are unsubstituted in the 3-position, but which may be substituted in the 4-position or beyond is disclosed.

    专利号:US-6146859-A
    优先权日:1999-08-27
    标题 :Facile synthesis of L-homophenylalanine by equilibrium shift enzymatic reaction using engineered tyrosine aminotransferase
    发明人:CHEN SHUI-TEIN; TSENG MIN-JEN; SOOKKHEO BOONYARAS
    权利人:ACADEMIA SINICA
    摘要:A process for producing L-homophenylalanine comprises the step of reacting 2-oxo-4-phenylbutyric acid with a L-amino acid in the presence of tyrosine aminotransferase in a reaction solution to produce L-homophenylalanine.

    专利号:US-5256552-A
    优先权日:1988-02-08
    标题 :Process for the production of optically active 2-hydroxy-4-phenylbutyric acid
    发明人:MATSUYAMA AKINOBU; NIKAIDO TERUYUKI; KOBAYASHI YOSHINORI
    权利人:DAICEL CHEM
    摘要:2-Oxo-4-phenylbutyric acid is treated with a microorganism, which has been optionally treated, capable of asymmetrically reducing 2-oxo-4-phenylbutyric acid into either (R)-2-hydroxy-4-phenylbutyric acid or (S)-2-hydroxy-4-phenylbutyric acid, and the (R)-2-hydroxy-4-phenylbutyric acid or (S)-2-hydroxy-4-phenylbutyric acid thus produced is recovered to thereby give optically active 2-hydroxy-4-phenylbutyric acid. n The optically active 2-hydroxy-4-phenylbutyric acid is an important intermediate in the synthesis of various drugs such as a remedy for hypertension.

    专利号:US-5686275-A
    优先权日:1991-12-23
    标 题 :Synthesis of homochiral 2-hydroxy acids
    发明人:CASEY GUY; LEE THOMAS; LEE ADMINISTRATOR VICTOR; LEE ADMINISTRATRIX EILEEN ANN
    权利人:GENZYME LTD
    摘要:PCT No. PCT/GB92/02396 Sec. 371 Date Aug. 26, 1994 Sec. 102(e) Date Aug. 26, 1994 PCT Filed Dec. 23, 1992 PCT Pub. No. WO93/13215 PCT Pub. Date Jul. 8, 1993A process for the production of a homochiral 2-hydroxy carboxylic acid or salt thereof corresponding to general formula (I), wherein R represents one of formulae (II), (III), (IV), (V), wherein R' represents straight- or branched-chain alkyl or phenyl optionally para-substituted with methyl, methoxy, nitro or amino; and R'' represents hydrogen, halogen or phenyl optionally para-substituted with methyl, methoxy, nitro or amino; and M represents hydrogen or a salt-forming moiety; characterized in that it comprises reducing a corresponding 2-keto carboxylic acid or salt thereof using a (R)- or (S)-2-oxo carboxylic acid dehydrogenase, inter alia, is disclosed.

    专利号:US-5371014-A
    优先权日:1988-02-12
    标题 :Process for the production of optically active 2-hydroxy acid esters using microbes to reduce the 2-oxo precursor
    发明人:MATSUYAMA AKINOBU; NIKAIDO TERUYUKI; KOBAYASHI YOSHINORI
    权利人:DAICEL CHEM
    摘要:An optically active 2-hydroxy acid derivative is produced by treating a 2-oxo acid derivative with a microorganism, which has been optionally treated, capable of asymmetrically reducing said 2-oxo acid derivative into an optically active (R)- or (S)-2-hydroxy acid derivative represented by the formula (II) and recovering the optically active (R)- or (S)-hydroxy acid derivative thus formed. Optically active 2-hydroxy acid derivatives are important intermediates in the synthesis of various drugs such as a remedy for hypertension.
    上海玛耀化学技术有限公司
    ⚠️ 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.mychems.com
    企业联系电话:021-51068321👤
    📞上海玛耀化学技术有限公司 ⚠️参考联系方式
    联系人:陈品岗
    电话:021-51068321

    传真:021-51068320
    邮箱:my@mychems.com
    通信地址: 上海市长安路1138号
    邮编: 200070
    🆔 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:上海市长安路1138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。
    上海凯赛化工有限公司
    ⚠️ 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.kaisaichem.com
    企业联系电话:021-33516711;33516722;13701817765👤
    📞上海凯赛化工有限公司 ⚠️参考联系方式
    联系人:殷小姐
    电话:021-33516711;33516722;13701817765
    手机:13701817765
    传真:QQ:56213393
    邮箱:kaisaichem@163.com
    通信地址: 上海市金沙江西路1051号
    邮编: 201803
    🆔 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:上海市金沙江西路1051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。
    上海蓝润化学有限公司
    ⚠️ 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.longrunchem.com
    企业联系电话:021-69515658;13701998368👤
    📞上海蓝润化学有限公司 ⚠️参考联系方式
    联系人:路小姐
    电话:021-69515658;13701998368
    手机:13701998368
    传真:QQ:819185261
    邮箱:longrunchem@163.com
    通信地址: 上海市青浦区重固镇赵重公路2278号5号楼4层C区34座
    邮编: 201800
    🆔 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:上海市青浦区重固镇赵重公路2278号5号楼4层C区34座
    ⚠️ 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。
    上海康拓化工有限公司
    ⚠️ 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.kangtuochem.com
    企业联系电话:021-69185552;69185553;13701777608👤
    📞上海康拓化工有限公司 ⚠️参考联系方式
    联系人:陈小姐
    电话:021-69185552;69185553;13701777608
    手机:13701777608
    传真:QQ:63651968
    邮箱:kangtuochem@163.com
    通信地址: 上海市嘉定区 沙河路
    邮编: 200000
    🆔 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:上海市嘉定区 沙河路
    ⚠️ 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。
    上海彤源化工有限公司
    ⚠️ 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.shtychem.com
    企业联系电话:021-69186366;69182866;13701855675👤
    📞上海彤源化工有限公司 ⚠️参考联系方式
    联系人:单小姐
    电话:021-69186366;69182866;13701855675
    手机:13701855675
    传真:QQ:89093626
    邮箱:tongyuanchem@126.com
    通信地址: 上海市青浦区重固镇赵重公路2278号5号楼3层E100座
    邮编: 201803
    🆔 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:上海市青浦区重固镇赵重公路2278号5号楼3层E100座
    ⚠️ 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。
    常州永和精细化学有限公司
    ⚠️ 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.yhchemical.com
    企业联系电话:13357885088👤
    📞常州永和精细化学有限公司 ⚠️参考联系方式
    联系人:陆先生
    电话:13357885088
    手机:13961122133;13961257237;13921086978
    传真:0519-88552298
    邮箱:service@yonghechemical.com
    通信地址: 常州市武进区洛阳镇戴溪东尖桥东
    邮编: 213105
    🆔 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:常州市武进区洛阳镇戴溪东尖桥东
    ⚠️ 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

    合成参考文献


    摘要:De Wildeman, S.; Sereinig, N., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 177.
    摘要:Zhou, Q.-Q.; Wei, Y.; Lu, L.-Q.; Xiao, W.-J., Science of Synthesis: Photocatalysis in Organic Synthesis, (2018) 1, 178.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 403.
    摘要:Parmeggiani, F.; Galman, J. L.; Montgomery, S. L.; Turner, N. J., Science of Synthesis, (2019) , 408.
    摘要:Zeitler, K., Science of Synthesis, (2019) , 292.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知