CAS: 87392-12-9; (S)-Metolachlor

该化合物是一种选择性除草剂,主要用于控制各种作物,特别是玉米和大豆的年草和某些大叶杂草,属于氯乙酸类除草剂和功能,抑制杂草在发芽和早期生长阶段生长;S-Metola氯的化学结构包括一个手艺中心,有助于针对目标杂草开展特定活动;其特征是,其挥发性较低,土壤吸附性高,有助于尽量减少渗入地下水;S-Metola氯通常在出血前或早期出血后应用,其效力可能受到土壤类型,湿度和温度等环境因素的影响;安全评估表明,根据标签指示使用S-Metola氯时,对非目标生物体,包括人类和野生动物,风险最小;但是,与所有农药一样,应谨慎处理,遵循适当的安全准则,以减少其使用可能带来的风险.

结构式图片

欧盟法规

[欧盟农药活性物质

上下游产品

CAS号79-04-9 氯乙酰氯 | CAS号118604-70-9 (S)-N-(2-ethyl-... | CAS号51219-00-2 2-ethyl-N-(2-me... | CAS号24549-06-2 2-甲基-6-乙基苯胺 | CAS号77-76-9 2,2-二甲氧基丙烷 | CAS号82508-03-0 (S)-(-)-N-(2-Et... | CAS号69516-03-6 N-(1'-methoxy-c... | CAS号82508-08-5 (S)-(-)-N-(1'-M... | CAS号87392-11-8 (aRS,1'S)-(+)-N...

合成工艺路线路线简述

  • 87392-11-8 + 77-76-9 = 87392-12-9
    反应条件:1.1 Catalysts: P-Toluenesulfonic Acid Solvents: Methanol; 36 H,Reflux
    标题:Chemoenzymatic Synthesis Of The Chiral Herbicide: (S)-Metolachlor
    作者:Zheng,Liangyu; Et Al
    参考文献:Canadian Journal Of Chemistry 日期:2006 卷标:84(8) 页码:1058-1063]

    87392-11-8 + 77-76-9 = 87392-12-9 [标题:Reaction Conditions
    标题:Effect Of Atropisomerism And Chiral Center On The Biological Activity Of Metolachlor
    作者:Moser,Hans; Et Al
    参考文献:Zeitschrift Fuer Naturforschung 日期:1982 卷标:(4) 页码:451-62]

    5878-19-3 + 24549-06-2 = 87392-12-9
    反应条件:1.1 Catalysts: Platinum Solvents: Water
    标题:(R)-1-[(1R)-1-(Dicyclohexylphosphino) Ethyl]-2-(Diphenylphosphino)-Ferrocene And (2S)-1-[(1R)-1-(Dicyclohexylphosphino)Ethyl]-2-(Diphenylphosphino)-Ferrocene (Josiphos)
    作者:Blaser,Hans-Ulrich; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2014 卷标:1 页码:1-21]

    132034-47-0 = 87392-12-9
    反应条件:1.1 Reagents: Hydrogen,Iodide Catalysts: Di-μ-Chlorobis[(1,2,5,6-η)-1,5-Cyclooctadiene]Diiridium,(2S)-1-[(1R)-1-[bis(1,1-Dimethylethyl)Phosphino]Ethyl]-2-(Dicyclohexylphosphino)... Solvents: Acetic Acid; 50 °C2.1 -
    标题:Hydrogen
    作者:Wilt,Jeremy C.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2016 卷标:1 页码:1-18]

    132034-48-1 = 87392-12-9
    反应条件:1.1 Catalysts: Borane,(4S)-4-(1-Methylethyl)-5,5-Diphenyl-1,3,2-Oxazaborolidine2.1 Catalysts: Sodium Bicarbonate
    标题:2-Amino-3-Methyl-1,1-Diphenyl-1-Butanol
    作者:Mathre,David J.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001]

    = 87392-12-9
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol; 1 H,Rt2.1 Reagents: Sodium Carbonate Solvents: Toluene; 0 °C; 1 H,Rt
    标题:An Efficient Synthesis Of Optically Active Herbicide (S)-Metolachlor Via Reductive Ring Opening Of 2-Methoxymethylaziridine
    作者:Nalla,Viswanadh; Et Al
    参考文献:Arkivoc (Gainesville 日期:2023 卷标:(6)
(S)-N-(2-Ethyl-6-Methylphenyl)Alanine置于dimethyl Sulfide Borane,Sodium Carbonate,对甲苯磺酸体系中,用 四氢呋喃,甲醇,苯 作为反应溶剂,化学反应 59.0H,反应生成 异丙甲草胺
参考文献:Der Einfluß Von Atropisomerie Und Chiralem Zentrum Auf Die Biologische Aktivität Des Metolachlor / Atropisomerism 和手性中心对 Metolachlor 生物活性的影响
标题:Der Einfluß Von Atropisomerie Und Chiralem Zentrum Auf Die Biologische Aktivität Des Metolachlor / Atropisomerism 和手性中心对 Metolachlor 生物活性的影响
摘要:制备了草除草剂异丙甲草胺的四种立体异构体,其异构体基于手性中心和手性轴的组合,并通过x射线分析确定了它们的绝对构型.该合成是通过使用光学活性起始材料和新的光学活性氨基甲酸酯作为中间体来实现的.除草活性主要受手性中心的影响,S-异构体是最活跃的.
DOI:10.1515/znb-1982-0411

海关参考信息

专利信息


专利号:WO-2024256370-A1
优先权日:2023-06-13
标 题 :Synthesis of glufosinate using an amidase-based process
发明人:ZIMMERMANN GUNTHER; POTT MORITZ STEFAN
权利人:BASF SE
摘要:The present invention relates to a method of preparing glufosinate, comprising the steps of hydrolysing an N-carbamoyl glufosinate amide with an Amidase enzyme to form an N- carbamoyl amino acid compound followed by cleaving off the carbamoyl moiety of said N- carbamoyl amino acid compound.

专利号:US-2025120400-A1
优先权日:2021-12-10
标题:Synthesis of glufosinate using a hydantoinase-based process
发明人:DITRICH KLAUS; BREUER MICHAEL; POTT MORITZ STEFAN; ZIMMERMANN GUNTHER; SEEMAYER STEFAN
权利人:BASF SE
摘要:The present invention relates to a method of manufacturing glufosinate, comprising the steps of hydrolysing a hydantoin with a Hydantoinase enzyme to form a N-carbamoyl amino acid compound followed by cleaving off the carbamoyl moiety of said N-carbamoyl amino acid compound.

专利号:WO-2007104357-A1
优先权日:2006-03-14
标 题 :Synthesis of amines with catalytic amounts of mild lewis acids
发明人:NUGENT THOMAS CHRISTOPHER; WAKCHAURE VIJAY NARAYAN; EL-SHAZLY MOHAMED MAHMOUD
权利人:UNIV JACOBS BREMEN GMBH; NUGENT THOMAS CHRISTOPHER; WAKCHAURE VIJAY NARAYAN; EL-SHAZLY MOHAMED MAHMOUD
摘要:The invention relates to methods for producing primary, secondary and tertiary amines and corresponding enantiopure or enantioenriched primary or secondary amine products, comprising the steps of reductively aminating a ketone, with a nitrogen auxiliary in the presence of a hydrogenating catalyst and a hydrogenating agent, wherein the reductive animation is performed under the influence of a mild Lewis acid, the mild Lewis acid being present at the onset of the reductive amination in at most 25 mol% of the ketone or the nitrogen auxiliary.

专利号:US-9199930-B2
优先权日:2012-09-06
标 题:Process for the preparation of (S)-2-ethyl-N-(1-methoxypropan-2-yl)-6-methyl aniline
发明人:MURUGAN MUTHUKRISHNAN; MUJUMDAR PRASHANT PRAMOD
权利人:COUNCIL SCIENT IND RES
摘要:Disclosed herein a novel, process for the preparation of (S)-2-ethyl-N-(1-methoxypropan-2-yl)-6-methyl aniline [(S)-1]. Particularly, the invention relates to the synthesis of (S)-2-ethyl-N-(1-methoxypropan-2-yl)-6-methyl aniline with excellent selectivity starting from commercially available enantiopure (R)-epichlorohydrin [(R)-2] via formation of aziridine intermediate [(S)-4].

专利号:US-11919928-B2
优先权日:2016-03-16
标题 :Method for producing dihydrotentoxin
发明人:KUBO TAKASHI; MACHIDA MASAYUKI; FUJIOKA TOMONORI; YAMAGUCHI Shigenari; KAWAI KIYOSHI
权利人:KUMIAI CHEMICAL INDUSTRY CO
摘要:An object of the present invention is to identify an enzyme having activity of synthesizing dihydrotentoxin that is a tentoxin precursor and an enzyme having activity of synthesizing tentoxin using dihydrotentoxin as a substrate. The present invention concerns a tentoxin synthesis-related gene encoding a protein comprising the amino acid sequence of SEQ ID NO: 16 and having activity of nonribosomal peptide synthesis of dihydrotentoxin and a tentoxin synthesis-related gene encoding a protein comprising the amino acid sequence of SEQ ID NO: 18 and having activity of converting dihydrotentoxin to tentoxin.

专利号:US-2021386068-A1
优先权日:2018-11-07
标题 :Compositions comprising pyridine carboxylate herbicides and very long chain fatty acid (vlcfa) synthesis inhibitor herbicides
发明人:KISTER JEREMY; SATCHIVI NORBERT M
权利人:CORTEVA AGRISCIENCE LLC
摘要:Disclosed herein are compositions comprising (a) a pyridine carboxylate herbicide or an agriculturally acceptable N-oxide, salt, or ester thereof and (b) a VLCFA synthesis inhibitor herbicide. Also disclosed herein are methods of controlling undesirable vegetation, comprising applying to vegetation or an area adjacent the vegetation or applying in soil or water to control the emergence or growth of vegetation (a) a pyridine carboxylate herbicide or an agriculturally acceptable N-oxide, salt, or ester thereof, and (b) a VLCFA synthesis inhibitor herbicide.
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摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
参考文献:10.1007/s11356-014-2876-x
摘要:Fauvelle V, Mazzella N, Morin S, Moreira S, Delest B, Budzinski H. Hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry for acidic herbicides and metabolites analysis in fresh water. Environmental Science and Pollution Research. 2014 May 27;22(6):3988–96. doi: 10.1007/s11356-014-2876-x.
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