CAS: 617-78-7; 3-Ethylpentane

该化合物是一种有机化合物,被归类为烷,具体地说是一种分环碳氢化合物,其分子式为C7H16,表明其由7个碳原子和16个氢原子组成,该化合物的五碳五角脊柱与三碳相连的乙基组相连,有助于其分支结构.3-乙基苯是一种无色液体,在室温下是一种无色液体,以其相对直链烷的粘度和挥发性相对较低而闻名.该化合物在水中溶解,但有机溶剂中溶性可溶性很强,因此在各种工业应用中有用,包括作为一种溶剂和燃料配制.该化合物有一个中度的沸点和闪点,典型的烷尺寸类似,易燃.此外,3-乙基苯烷可以通过各种方法合成,包括低烷的烷烷烷的正烷酸性,其特性使其对有机化学和石化工业的学术研究和实际应用都感兴趣.

结构式图片

欧盟法规

统一分类与标签压力设备指令-第1组危险流体ECHA物质欧盟气雾剂指令-标签制度工作场所安全标识要求ECHA物质C&L通报REACH预注册废弃物危险特性清单

上下游产品

2-甲基丁烷 Methylbutane 78-78-4
乙基环戊烷 Ethylcyclopentane 1640-89-7

合成工艺路线路线简述

    📜乙基环戊烷置于铂体系中,460.0 °C,1.96 Mpa 条件下,反应生成 3-乙基戊烷
    参考文献:Minatschew Et Al.,Doklady Akademii Nauk Sssr,1954,Vol. 99,P. 777,780
    标题:Minatschew Et Al.,Doklady Akademii Nauk Sssr,1954,Vol. 99,P. 777,780

    海关参考信息

    专利信息


    专利号:US-2006128930-A1
    优先权日:2004-12-03
    标题 :Synthesis of sterically hindered phenol based macromolecular antioxidants
    发明人:DHAWAN ASHISH; CHOLLI ASHOK L
    权利人:DHAWAN ASHISH; CHOLLI ASHOK L
    摘要:Disclosed is a method for the synthesis of sterically hindered polymeric antioxidants based on phenol type antioxidant monomers. The method includes polymerizing and alkylating a phenol containing monomer represented by the following structural formula: n n nto produce a sterically hindered polymeric macromolecular antioxidant. X, R 10 and q are as defined herein. The disclosed method is a simple, direct and economical process for the synthesis of sterically hindered polymeric macromolecular antioxidants.

    专利号:US-7678877-B2
    优先权日:2004-12-03
    标题 :Process for the synthesis of polyalkylphenol antioxidants
    发明人:YANG SUIZHOU; CHOLLI ASHOK L
    权利人:POLNOX CORP
    摘要:Disclosed is a method for the synthesis of sterically hindered polymeric antioxidants based on phenol type antioxidant monomers. The method includes partially etherifying, polymerizing and thermally rearranging a phenol containing monomer represented by the following structural formula: n nto produce a sterically hindered polymeric macromolecular antioxidant. X, R 10 and q are as defined herein. The disclosed method is a simple, direct and economical process for the synthesis of sterically hindered polymeric macromolecular antioxidants.

    专利号:US-2003162992-A1
    优先权日:2001-12-14
    标 题 :Preparation of intermediates useful in the synthesis of antiviral nucleosides
    发明人:WATANABE KYOICHI A; DU JINFA
    摘要:The present invention is an efficient process for the manufacture of α-acyloxyacetaldehyde, a key intermediate in the synthesis of 1,3-oxathiolane and 1,3-dioxolane nucleosides.

    专利号:US-2008125587-A1
    优先权日:2006-05-25
    标 题 :Synthesis of triazole compounds that modulate HSP90 activity
    发明人:CHIMMANAMADA DINESH U; LEE CHI-WAN; JAMES DAVID; ZHANG SHIJIE; YING WEIWEN; CHAE JUNGHYUN; PRZEWLOKA TERESA
    权利人:CHIMMANAMADA DINESH U; LEE CHI-WAN; JAMES DAVID; ZHANG SHIJIE; YING WEIWEN; CHAE JUNGHYUN; PRZEWLOKA TERESA
    摘要:The present invention provides novel methods of preparing triazole compounds which inhibit the activity of Hsp90. One embodiment of the invention is directed to methods for preparing a triazole compound represented by the following Structural Formula: n n n n n n n n n n or a tautomer, a pharmaceutically acceptable salt, solvate, or clathrate, or a prodrug thereof, comprising the steps of: a) reacting an amide represented by the following Structural Formula: n n n n n n n n n n with a thionation reagent to form a thioamide; b) reacting the thioamide of step a) with hydrazine to form a hydrazonamide; c) reacting the hydrazonamide of step b) with a carbonylation or a thiocarbonylation reagent. n In one embodiment, the present invention is a method of synthesis of a compound of formula (IA) n n n n n n n n n n or a tautomer, a pharmaceutically acceptable salt, solvate, or clathrate, or a prodrug thereof, comprising reacting a compound of formula (IIA) n n n n n n n n n n with an oxidizing agent, thereby producing a compound of formula (IA). n The present invention is also directed to a method of preparing a compound or a tautomer thereof represented by the following Structural Formula: n n n n n n n n n n or a tautomer, a pharmaceutically acceptable salt, solvate, or clathrate, or a prodrug thereof. The method comprises the step of reacting a first starting compound represented by the following Structural Formula: n n n n n n n n n n in the presence of a mercuric salt, with a second starting compound represented by the following Structural Formula:

    专利号:WO-2024246574-A1
    优先权日:2023-06-02
    标题:METHOD OF SYNTHESIS OF COLLOIDAL InSb QUANTUM DOTS
    发明人:REISS PETER; KWON YONGJU
    权利人:COMMISSARIAT A LENERGIE ATOMATIQUE ET AUX ENERGIES ALTERNATIVES; CENTRE NAT RECH SCIENT; UNIV GRENOBLE ALPES
    摘要:The present invention relates to a method of synthesis of colloidal InSb quantum dots (InSb QDs) comprising a premixing step of In and Sb precursors at a temperature of less than 100°C, under stirring.

    专利号:US-7767826-B2
    优先权日:2007-10-05
    标题 :Process for the synthesis of L-(+)-ergothioneine
    发明人:TRAMPOTA MIROSLAV
    权利人:PHARMATECH INTERNATIONAL INC
    摘要:This invention relates to a novel process for the preparation of optically pure L-(+)-ergothioneine. The process for the chemical synthesis of L-ergothioneine comprises steps which consist of reacting L-histidine alkyl ester with an acid halide, chloroformate or pyrocarbonate in the presence of a base, hydrolysis of the alkyl-(S,Z)-2,4,5-triamidopent-4-enoate to obtain a (S)-alkyl 2,5-diamido-4-oxopentanoate, acid catalyzed hydrolysis of the (S)-alkyl 2,5-diamido-4-oxopentanoate followed by reaction with a metal thiocyanate to obtain the thiohistidine, protection of the sulfur of thiohistidine as the tert-butyl thioether, dialkylation of the primary amine to obtain a tertiary amine, quaternization of the tertiary amine, and removal of the protecting group to obtain the desired (S)-3-(2-mercapto-1H-imidazol-5-yl)-2-(trialkylammonio)propanoate (I). This process affords a better yield and is capable of practical application at large scale.

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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:Wicha, J., Science of Synthesis, (2009) 48, 167.
    摘要:Molnár, Á., Science of Synthesis, (2009) 48, 469.
    摘要:Caballero, A.; Díaz-Requejo, M. M.; Pérez, P. J., Science of Synthesis: Catalytic Oxidation in Organic Synthesis, (2017) 1, 182.
    摘要:L400: Wikipedia. Lead telluride. Last Updated 8 May 2009.
    摘要:T29: Bingham, E, Cohrssen, B, and Powell, CH (2001). Patty's Toxicology Volumes 1-9. 5th ed. New York, N.Y: John Wiley & Sons.
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