CAS: 107-39-1; 2,4,4-Trimethyl-1-Pentene

该化合物是一种有机化合物,被归类为烷,其特点是不饱和碳氢化合物结构,具有双重结合;其分子式为C8H16,表明含有8个碳原子和16个氢原子;该化合物一般是一种无色液体,在室温下具有独特的气味;其结构包括一个附着三个甲基组的钢柱,有助于其分支性质;2,4,4-三甲基-1-五苯,因其反应性,特别是聚合反应,使其在生产各种聚合物和化学中间体时有用;该化合物还用于有机合成,可作为制造其他化学化合物的建筑块;该化合物在标准条件下相对稳定,但可能会发生典型的藻类反应,例如附加反应;在处理该物质时,应当采取安全防范措施,因为它可能是易燃的,并且会在与皮肤或眼睛接触时引起刺激.

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

CAS号115-11-7 2-甲基丙烯 | CAS号540-88-5 醋酸叔丁酯 | CAS号107-40-4 2,4,4-三甲基-2-戊烯 | CAS号187737-37-7 propene | CAS号111-66-0 1-辛烯 | CAS号5162-48-1 2,2,4-三甲基-3-戊醇 | CAS号690-37-9 2,4,4-三甲基-2-戊醇 | CAS号107-45-9 叔辛胺 | CAS号38442-51-2 tert-butyl(chlo... | CAS号563-47-3 3-氯-2-甲基-1-丙烯(MAC) | CAS号107-48-2 Oxirane,2-(2,2-... | CAS号78950-58-0 tetrachloroacet... | CAS号590-50-1 4,4-二甲基-2-戊酮 | CAS号114448-05-4 1-Hydroperoxy-2... | CAS号64484-85-1 1,2-Pentanediol... | CAS号17414-46-9 2,4,4-trimethyl... | CAS号98-51-1 4-叔丁基甲苯 | CAS号1074-92-6 2-叔丁基甲苯

合成工艺路线路线简述

    2,4,4-三甲基-2-戊烯置于dibromo(Dimethylglyoxime)(Dimethylglyoximato)Cobalt(III),Sodium Decatungstate体系中,用 乙腈 用作溶剂,化学反应 18.0H,以85%的收率获得异辛烯
    参考文献:催化,逆热力学位置烯烃异构化
    标题:催化,逆热力学位置烯烃异构化
    摘要:C=c双键的位置异构化是烯烃区域异构体相互转化的有力策略.然而,现有方法提供了从不太稳定的起始材料获得热力学上更稳定的异构体的途径.在这里,我们报告了在光化学辐照下促进逆热力学位置烯烃异构化的双催化剂系统的发现,提供了直接从共轭的内部烯烃起始材料获得末端烯烃异构体的途径.该方法的实用性在多种富电子/贫电子烯烃的去共轭中以及通过对天然产物合成的战略应用得到证明.机理研究与区域特异性双分子均裂取代(s H2') 机制通过烯丙基钴肟中间体进行.
    Doi:10.1021/jacs.1C12043

    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-6800783-B2
    优先权日:2000-03-04
    标题:Method for the synthesis of aliphatic carboxylic acids from aldehydes
    发明人:SPRINGER HELMUT; LAPPE PETER
    权利人:CELANESE CHEM EUROPE GMBH
    摘要:The invention relates to a method for the synthesis of aliphatic carboxylic acids by the catalytic oxidation of aldehydes with oxygen, or oxygen-containing gas mixtures. Metals of groups 5 11 of the periodic table of elements, or the compounds thereof are used as catalyst, in amounts of up to 5 ppm, based upon the amount of aldehyde used.

    专利号:US-4891445-A
    优先权日:1987-02-17
    标题 :Synthesis of tertiary mercaptans from isobutylene homopolymers
    发明人:ARRETZ EMMANUEL
    权利人:ELF AQUITAINE
    摘要:The invention relates to the synthesis of tertiary mercaptans from isobutylene homopolymers and from hydrogen sulphide by means of heterogeneous catalysis. In the processs according to the invention, the reaction is carried out at a temperature below 45 DEG C., preferably between 0 DEG and 35 DEG C., in the presence of a catalyst consisting of a dry cation exchange resin. Excellent yields of tertiary mercaptan are thus obtained, while the formation of undesirable byproducts is virtually avoided.

    专利号:US-3647837-A
    优先权日:1970-02-09
    标 题 :Synthesis of organolead compounds
    发明人:WILLIAMS KENNETH C
    权利人:ETHYL CORP
    摘要:A METHOD OF MAKING ORGANOLEAD COMPOUNDS AND PARTICULARLY THE SYNTHESIS OF TETRANEOPENTYLLEAD AND HEXANEOPENTYLDILEAD FROM AN INORGANIC LEAD (II) SALT, AND THE USE OF SAID LEAD COMPOUNDS FOR DECREASING KNOCK IN INTERNAL COMBUSTION ENGINES.

    专利号:US-5780689-A
    优先权日:1991-07-10
    标题 :Superacidic catalysts for the synthesis of methyl-tert-butyl ether (MTBE)
    发明人:MAO RAYMOND LE VAN
    权利人:QUEBECOISE D INITIATIVES PETRO
    摘要:In accordance with the present invention, there is now provided a novel selective catalyst useful for the synthesis of methyl-tert-butyl ether (MTBE) or ethyl-tert-butyl ether (ETBE) prepared by reacting isobutene with methanol or ethanol, respectively. More specifically, the catalyst of the present invention comprises from about 0.5 to about 7% by weight of triflic acid (trifluoro-methanesulfonic acid, CF3SO3H, hereafter referred to as TFA) incorporated onto an acid form Y zeolite.
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    主要参考文献

    参考标题:Synthesis And Photophysics Of Dibenz[A,C]Phenazine Derivatives
    作者:Leandro A. Estrada,Douglas C. Neckers |发布日期:2011.7.1
    摘要:The Synthesis Of Dipolar Dibenz[a,C]Phenazine (Dbp) Derivatives Is Described. The Compounds Possess Little Electronic Communication Between Donor And Acceptor Units In The Ground State Regardless Of The Pattern Of Substitution. The Dipolar Derivatives Deactivate Mostly Via Electron Transfer (Et) Under Polar Conditions. Intersystem Crossing Is Likely To Compete For S1 Relaxation.

    合成参考文献


    摘要:Kostikov, R. R.; Khlebnikov, A. F.; Sokolov, V. V., Science of Synthesis, (2010) 47, 792.
    摘要:Kostikov, R. R.; Khlebnikov, A. F.; Sokolov, V. V., Science of Synthesis, (2010) 47, 780.
    摘要:Kantchev, E. A. B.; Organ, M. G., Science of Synthesis, (2009) 48, 10.
    摘要:Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 79th ed. Boca Raton, FL: CRC Press Inc., 1998-1999., p. 3-248
    摘要:Fire Protection Guide to Hazardous Materials. 12 ed. Quincy, MA: National Fire Protection Association, 1997., p. 491-74
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