CAS: 1123-25-7; 1-Methylcyclohexanecarboxylic Acid

该化合物是一种环氧碳箱酸,其特征是环氧环乙烷环状,代之以一个甲基组,以及一个碳箱酸功能组,该化合物一般看起来无色可粉黄色液体或固体,视温度和纯度而定,在水中具有相对较低的沸点和中度溶解性,这在箱状酸中很常见,因为箱状酸能够形成氢结壳.甲基酸的存在会影响其物理特性,如挥发性和再活动.1-M乙基环己烷箱酸可以参与各种化学反应,包括酯化和脱色反应,使其在有机合成中有用.其结构特征有助于其在芳香,制药和农用化学品生产中的潜在应用.安全数据表明,与许多有机酸一样,它应该谨慎处理,以避免皮肤和眼刺激.

结构式图片

相似化合物

14064-13-2 62718-34-7 6553-85-1

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

4-(1-methylcyclohexyl)phenol 1-methylcyclohexanecarbonitrile cycloheptanol trans-4-methylcyclohexan-1-ol (1-methylcyclohexyl)methanol 1-methyl-1-cyclohexylamine 1-methyl-1-cyclohexancarboxylic acid chloride methyl 1-methylcyclohexanecarboxylate

合成工艺路线路线简述

  • 合成目标产物 1-Methyl-1-Cyclohexanecarboxylic Acid 主要起始原料 Formic Acid And 1-Chloro-1-Methylcyclohexane
  • (文献来源)合成步骤主要原料 Formic Acid 和 1-Chloro-1-Methylcyclohexane
乙酰基环己烷置于氢氧化钾,磺酰氯体系中,用 乙醇 用作溶剂,化学反应生成1-甲基环己烷羧酸
参考文献:Rouzaud,J. Et Al.,Bulletin De La Societe Chimique De France,1964,P. 2908-2916
标题:Rouzaud,J. Et Al.,Bulletin De La Societe Chimique De France,1964,P. 2908-2916

海关参考信息

专利信息


专利号:WO-2015018845-A1
优先权日:2013-08-08
标题:Method for the synthesis of saturated carboxylic acid esters
发明人:WU MSC LIPENG; BELLER MATTHIAS; JACKSTELL RALF; LIU QIANG; FLEISCHER IVANA
权利人:LEIBNIZ INST FÜR KATALYSE E V AN DER UNIVERSITÄT ROSTOCK
摘要:The invention relates to a method for the synthesis of saturated carboxylic acid esters, wherein corresponding C1 truncated alkenes are reacted with an alcohol in the presence of carbon dioxide and a catalyst based on ruthenium.

专利号:US-2006052577-A1
优先权日:2001-02-06
标题:Methods of synthesis of polymers and copolymers from natural products
发明人:SWIFT GRAHAM; WESTMORELAND DAVID G; HUGHES KATHLEEN
权利人:SWIFT GRAHAM; WESTMORELAND DAVID G; HUGHES KATHLEEN
摘要:Described are polymers and copolymers containing sorbitol, citric acid, starch, aspartic acid, succinic anhydride, adipic acid mixtures thereof, methods of their synthesis and their uses.

专利号:US-6011171-A
优先权日:1996-08-14
标 题 :Process for synthesis of tertiary carboxylic acids and the esters thereof
发明人:XU QIANG; SOUMA YOSHIE
权利人:JIRO HIRAISHI DIRECTOR GENERAL
摘要:The present invention provides a process for synthesizing tertiary carboxylic acids or the esters thereof having one or two more carbon atoms than the raw material has, comprising reacting in a strong acid (e.g., sulfuric acid, sulfuric acid-phosphoric acid, hydrogen fluoride, fluorosulfuric acid, boron trifluoride.water complex and trifluoromethanesulfonic acid) a raw material compound (i.e., olefin, alcohol, diene, diol or saturated hydrocarbon) with carbon monoxide in the presence of a specific metal carbonyl catalyst (i.e., platinum carbonyl catalyst, palladium carbonyl catalyst and gold dicarbonyl catalyst). The metal carbonyl catalyst is formed by reacting in a strong acid at least one specific metal compounds (e.g., platinum compound such as platinum (II, IV) oxide, platinum (II, IV) hydroxide, a platinum powder, etc.; palladium compound such as palladium (II, III, IV) oxide, palladium (II) hydroxide, palladium (II) sulfate, palladium (II) carboxylate, a palladium powder, etc.; and gold compound such as gold (I, III) oxide, gold (I, III) hydroxide, a gold powder, etc.) with carbon monoxide.

专利号:WO-2015131100-A1
优先权日:2014-02-28
标题:Ligand-controlled c(sp3)-h arylation and olefination in synthesis of unnatural chiral alpha amino acids
发明人:YU JIN-QUAN
权利人:SCRIPPS RESEARCH INST
摘要:The use of ligands to tune the reactivity and selectivity of transition metal-catalysts for C(-sp3)-H bond functionalization is a central challenge in synthetic organic chemistry. Herein, we report a rare example of catalyst-controlled C(sp3)-H arylation using pyridine and quinoline derivatives: the former promotes exclusive monoarylation, whereas the latter activates the catalyst further to achieve diarylation. Successive application of these ligands enables the sequential diarylation of a methyl group in an alanine derivative with two different aryl iodides, affording a wide range of β-Ar-p-Ar ' -cc-amino acids with excellent levels of diastereoselectivity (d.r. > 20:1). Both configurations of the β-chiral center can be accessed by choosing the order in which the aryl groups are installed. The use of a quinoline derivative as a ligand also enables C(sp3)-H olefination of a protected alanine.

专利号:US-2005261474-A1
优先权日:2004-05-20
标题:Method of support-based chemical synthesis
发明人:HOUGHTEN RICHARD A; YU YONGPING
权利人:MIXTURE SCIENCES INC
摘要:A method of synthesis on a solid phase support is disclosed that provides a cleaved product containing a protecting group that would have been cleaved by reaction with anhydrous HF wherein the support is volatilized during cleavage of the protected product from the support by reaction with diluted HF.

专利号:US-6531470-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人:GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
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主要参考文献

[参考文献]: A J Sadeque, Et Al. Human Cyp2C9 And Cyp2A6 Mediate Formation Of The Hepatotoxin 4-Ene-Valproic Acid. J Pharmacol Exp Ther. 1997 Nov;283(2):698-703.
[参考文献]: J C Larcher, Et Al. Regulation Of C- And N-Myc Expression During Induced Differentiation Of Murine Neuroblastoma Cells. Oncogene. 1991 Apr;6(4):633-8.
[参考文献]: J L Vayssière, Et Al. Is The Induction Of Neuroblastoma Differentiation By Cca Mediated By Its Effects On The Electrochemical Gradient. Febs Lett. 1984 Jul 23;173(1):19-22.
[参考文献]: M J Liu, Et Al. Pharmacokinetics And Pharmacodynamics Of Valproate Analogs In Rats. Ii. Pharmacokinetics Of Octanoic Acid, Cyclohexanecarboxylic Acid, And 1-Methyl-1-Cyclohexanecarboxylic Acid. Biopharm Drug Dispos. 1993 May;14(4):325-39.
[参考文献]: M J Liu, Et Al. Pharmacokinetics And Pharmacodynamics Of Valproate Analogs In Rats. Iii. Pharmacokinetics Of Valproic Acid, Cyclohexanecarboxylic Acid, And 1-Methyl-1-Cyclohexanecarboxylic Acid In The Bile-Exteriorized Rat. Drug Metab Dispos. 1992 Nov-Dec;20(6):810-5.

合成参考文献


摘要:Muralirajan, K.; Rueping, M., Science of Synthesis, (2019) , 347.
摘要:de Figueiredo, R. M., Science of Synthesis: Knowledge Updates, (2024) 2, 275.
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