CAS: 626-89-1; 4-Methylpentan-1-Ol

该化合物是一种该化合物是一种清晰的无色液体,有温味,通常用作有机合成和特殊化学生产的中间体,其分流结构有助于降低线性酒精的挥发性,使之适合需要控制反应的用途.由于该化合物具有中度极度和溶解性,该化合物还被用作溶剂或调味剂.关键优点包括其在标准条件下的稳定性和与各种工业工艺的兼容性.其合成通常涉及水成或灰度反应,确保技术和实验室用途的高纯度.

结构式图片

相似化合物

25415-67-2 2412-80-8 646-07-1

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

oxirane isobutylmagnesium bromide di-iso-butylmagnesium isobutylmagnesium iodide Mono-isohexyl phthalate 1-iodo-4-methylpentane 4-Methyl-1-pentene 4-Methylpentanoic acid Alcohols ( Methyl isobutyl carbinol 2-ethoxy-1-bromo-4-methyl-pentane 4-Methyl-1-pentanol 4-methyl-2-pentyl acetate propene methane ethane ethene

合成工艺路线路线简述

  • 56-81-5 = 626-89-1 + 1191-25-9 + 627-98-5 + 111-29-5 + 4048-33-3 + 13392-69-3 + 927-55-9 + 928-40-5 + 13325-10-5 + 2508-29-4 + 629-11-8 + 110-63-4 + 626-95-9
    反应条件:1.1 Reagents: Calcium Pantothenate,Mops,Disodium Phosphate,Ferrous Sulfate,Ammonium Sulfate,Ammonium Chloride Catalysts: Acetyl Coenzyme A Acetyltransferase,Acyl Coenzyme A Dehydrogenase,3-Hydroxyacyl Coenzyme A Dehydrogenase,Alcohol Dehydrogenase,Fatty Acyl Coenzyme A Reductase (Aldehyde-Forming) Solvents: Water; 37 °C
    标题:Production Of Functionalized Carboxylic Acids And Alcohols By Reverse Fatty Acid Oxidation In Metabolically Engineered Microorganisms
    参考文献:United States
异己烯置于c33H58Con3Psi2,1,3-二甲基-1,3,2-二氮杂硼杂环戊烷体系中,用 Neat (No Solvent) 作为反应溶剂,化学反应 18.0H,反应生成 4-甲基-1-戊醇
参考文献:钴和铁催化的异构化-支链烯烃的加氢硼化:品加烷硼烷和1,3,2-二氮杂硼烷的末端硼氢化
标题:钴和铁催化的异构化-支链烯烃的加氢硼化:品加烷硼烷和1,3,2-二氮杂硼烷的末端硼氢化
摘要:The Synthesis And Characterization Of A Series Of Structurally Varied N-Phosphinoamidinate-Ligated Cobalt Complexes Is Described,Along With The Successful Application Of These And A Related Iron Complex As Precatalysts In The Isomerization Hydroboration Of Terminal,Geminal,And Internal Alkenes. These Reactions Proceed Under Mild Conditions (23-65 Degrees C),At Relatively Low Base-Metal Loadings (1-5 Mol %),Typically Without Cosolvent,And With High Terminal Hydroboration Selectivity Across A Broad Spectrum Of Branched Alkenes. With Some Of The Alkene Substrates Examined,The Nphosphinoamidinate-Ligated Precatalysts Employed Herein Are Shown To Provide Alternative Terminal Selectivity Versus Other Previously Reported Precatalyst Classes For Such Transformations. Reports Of Terminal-Selective Metal-Catalyzed Alkene Isomerization Hydroboration Disclosed Thus Far In The Literature Employ Pinacolborane (Hbpin); While Effective In The System Herein,We Also Report The First Examples Of Such Transformations Employing Either 1,3-Dimethyl-1,3-Diaza-2-Boracydopentane Or Benzo-1,3,2-Diazaborolane. The Application Of These 1,3,2-Diazaborolanes In Place Of Hbpin In Some Instances Enables Novel Terminal Selectivity In The Isomerization Hydroboration Of Branched Alkenes.
DOI:10.1021/acs.Organomet.6B00823

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主要参考文献

[参考文献]: Selli S, Et, Al. Volatile Composition Of Red Wine From Cv. Kalecik Karasι Grown In Central Anatolia
[参考文献]: Shujuan Zhang, Et Al. Influence Of Pre-Fermentation Treatments On Wine Volatile And Sensory Profile Of The New Disease Tolerant Cultivar Solaris. Molecules. 2015 Dec 3;20(12):21609-25.

合成参考文献

参考DOI号:10.1021/acs.j°C.7b02993
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