CAS: 97-96-1; 2-Ethylbutyraldehyde

该化合物是一种有机化合物,被归类为aldhydy;C6H12O分子分子式,具有五碳脊柱和与第二碳相连的乙基组;该化合物一般是一种无色液体,具有典型的气味,通常被称为果味或甜味;有机溶剂中溶解,并且由于水分碳氢化合物链,水溶解性有限. 2-乙基丁烷因其活性而闻名,特别是在进行相应的碳酸氧化或参与各种凝聚反应时;它用于其他有机化合物的合成,并且可在某些调味剂和香味中找到.安全考虑包括在通风良好的地区处理它,因为它可能会对皮肤,眼睛和呼吸系统产生刺激.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号106-98-9 正丁烯 | CAS号201230-82-2 carbon monoxide | CAS号845791-28-8 1,1-diacetoxy-2... | CAS号66-25-1 正己醛 | CAS号97-95-0 2-乙基-1-丁醇 | CAS号31499-97-5 2-ethyl-N,N-dim... | CAS号646-04-8 反-2-戊烯 | CAS号2736-40-5 2-乙基丁酰氯 | CAS号105438-31-1 3-(2-ethylbut-1... | CAS号37577-28-9 左旋去甲麻黄碱 | CAS号143818-53-5 4-((4-carboxyph... | CAS号14086-21-6 Butanal, 2-ethy... | CAS号19781-29-4 3-乙基-4-辛酮 | CAS号19781-28-3 3-ethyl-4-°Ctanol | CAS号21020-26-8 3-ethylpent-1-yne | CAS号28478-26-4 Morpholine,4-(2... | CAS号106-70-7 己酸甲酯

合成工艺路线路线简述

    2-乙烯基-2-丁烯醛置于nickel Diacetate,铁粉,溶剂黄146体系中,化学反应生成 2-乙基丁醛
    参考文献:Zeisel; Neuwirth,Justus Liebigs Annalen Der Chemie,1923,Vol. 433,P. 126
    标题:Zeisel; Neuwirth,Justus Liebigs Annalen Der Chemie,1923,Vol. 433,P. 126

    海关参考信息

    专利信息


    专利号:US-2010099894-A1
    优先权日:2006-10-09
    标 题 :Method for the Synthesis of Cyclic Acetals by the Reactive Extraction of a Polyol in a Concentrated Solution
    发明人:DUBOIS JEAN-LUC; IBORRA CHORNET SARA; VELTY ALEXANDRA I LUCIENNE; CORMA CANOS AVELINO
    权利人:DUBOIS JEAN-LUC; IBORRA CHORNET SARA; VELTY ALEXANDRA I LUCIENNE; CORMA CANOS AVELINO
    摘要:A method for the synthesis of cyclic acetals comprises reacting at least one carbonyl-function compound selected from aldehydes, ketones, and/or linear acetals, on a polyol in a concentrated aqueous solution exceeding 20 wt % in a reactor containing an acidic catalyst. The carbonyl-function compound is selected so that the cyclic acetal obtained has a water solubility lower than 20000 mg/kg. During the catalytic reaction for the cyclic acetal synthesis, at least one portion of the organic phase containing the cyclic acetal is separated. The acidic catalysis is either homogeneous when using a water-soluble strong acid, or heterogeneous when using a solid acid such as a resin, a zeolite, or any appropriately acidified solid. The extractive reaction method can be used for obtaining high conversions and selectivity.

    专利号:US-9403841-B2
    优先权日:2012-01-25
    标题:Phragamalin limonoids for the treatment of sexual dysfunction
    发明人:WIKBERG JARL; JIRGENSONS AIGARS; LIEPINSH EDVARDS
    权利人:DICOTYLEDON AB
    摘要:The present invention relates to novel chemical compounds, to methods for synthesis of such compounds, and to the use of these novel compounds in the synthesis of other chemical compounds that, inter alia, may be used in the treatment of sexual dysfunction, and for eliciting enhancing effects on sexual behavior. The invention also relates to remarkable biological properties of the novel compounds in their capacity of inducing aggressive behavior.

    专利号:US-6358928-B1
    优先权日:1999-11-22
    标 题 :Peptidyl sulfonyl imidazolides as selective inhibitors of serine proteases
    发明人:RASNICK DAVID W
    权利人:ENZYME SYSTEMS PRODUCTS
    摘要:Novel alpha-amino and peptidyl sulfonyl imidazolides, a method for their synthesis, and a method for inhibiting serine proteases therewith are disclosed. Pharmaceutical compositions containing alpha-amino and peptidyl sulfonyl imidazolides and their use in the treatment of disease states characterized by an over-activity of serine proteases are also disclosed. Novel synthetic methods for the synthesis of sulfonyl derivatives, particularly alpha-amino and peptidyl sulfonyl derivatives, from thioic acid S-esters are also disclosed.

    专利号:WO-0212185-A1
    优先权日:2000-08-10
    标 题:Process for preparing 2,3-diaminopropanols and synthesis of other compounds using 2,3-diaminopropanols
    发明人:LEE WON KOO; SHIN SEONG-HO; HA HYUN-JOON
    权利人:CHEMBIONEX CO LTD; HANSOL CHEMIENCE CO LTD; LEE WON KOO; SHIN SEONG HO; HA HYUN JOON
    摘要:The invention relates to a process for producing 2,3-diaminopropanol of formula (II) from aziridine of formula (I) wherein, R1 is selected from a group consisting of hydrogen, alkyl, cycloalkyl, acyl, aryl, hydrocarbon residues, aralkyl, and those groups substituted with suitable substituent(s); R2 is selected from a group consisting of hydrogen, alkyl, cycloalkyl, C¿2?-C5-alkenyl, aralkyl which may be optionally substituted with suitable substituent(s), aryl which may be optionally substituted with suitable substituent(s), and heteroaryl which may be optionally substituted with suitable substituent(s); each of R?3 and R4¿ is independently selected from a group consisting of hydrogen, C¿1?-C12 alkyl, C1-C12 alkylcarbonyl, C1-C12 alkyloxycarbonyl, aryl, mono- or di(C1-C12)alkylamino, mono- or di(C1-C12)amino carbonyl, wherein C1-C12 may be optionally substituted, or R?3 and R4¿, together with nitrogen atom which they are attached to, may form pyrrolidinyl, piperidinyl, morpholinyl, azido or mono- or di(C¿1?-C12)alkylamino C1-C4 alkylidene.

    专利号:US-9018387-B2
    优先权日:2010-06-11
    标 题:Complexes of imidazole ligands
    发明人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; LEI XINJIAN; SPENCE DANIEL P; IVANOV SERGEI VLADIMIROVICH; BAILEY III WADE HAMPTON
    权利人:NORMAN JOHN ANTHONY THOMAS; PEREZ MELANIE K; LEI XINJIAN; SPENCE DANIEL P; IVANOV SERGEI VLADIMIROVICH; BAILEY III WADE HAMPTON; AIR PROD & CHEM
    摘要:Metal imidazolate complexes are described where imidazoles ligands functionalized with bulky groups and their anionic counterpart, i.e., imidazolates are described. Compounds comprising one or more such polyalkylated imidazolate anions coordinated to a metal or more than one metal, selected from the group consisting of alkali metals, transition metals, lanthanide metals, actinide metals, main group metals, including the chalcogenides, are contemplated. Alternatively, multiple different imidazole anions, in addition to other different anions, can be coordinated to metals to make new complexes. The synthesis of novel compounds and their use to form thin metal containing films is also contemplated.

    专利号:US-5270468-A
    优先权日:1992-04-01
    标 题 :2- and 3- amino azido derivatives of 1,5-iminosugars
    发明人:KHANNA ISH K; MUELLER RICHARD A; WEIER RICHARD M; STEALEY MICHAEL A
    权利人:SEARLE & CO
    摘要:Novel derivatives of 1-deoxynojirimycin are disclosed which have amino or azido substituents at C-2 and/or C-3. These compounds are useful inhibitors of lentiviruses. Methods of chemical synthesis of these derivatives and intermediates therefor are also disclosed.
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    合成参考文献


    摘要:Wu, X.-F., Science of Synthesis Knowledge Updates, (2014) 1, 255.
    摘要:Nahm Garrett, M.; Johnson, J. S., Science of Synthesis Knowledge Updates, (2012) 2, 8.
    摘要:Molander, G. A.; Beaumard, F., Science of Synthesis Knowledge Updates, (2013) 3, 132.
    摘要:Joule, J. A., Science of Synthesis Knowledge Updates, (2010) 2, 193.
    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 217.
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