CAS: 20193-21-9; N-Propylbutan-1-Amine

该化合物是一种有机化合物,被归类为一种矿物质;它具有直链结构,由附于氮原子的一个丁基组组成,该组也与一个丙基组捆绑在一起;该组的特征是其脂质性质,它有助于有机溶剂中相对较低的沸点和中度溶解性;N-Propyl-1-butanamine展示了氨的典型基本特性,允许它参与各种化学反应,包括核生殖器替代和串联;它还可能由于矿体功能组的存在而参与氢联,影响其物理特性和再活动;该组对有机合成感兴趣,并可作为生产药品或农用化学品的一种中间体;在处理和储存时,应参考安全数据,因为氨可能是刺激剂,如果管理不当,可能会对健康造成危害.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

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CAS号7707-71-3 butylidene-prop... | CAS号54509-73-8 ethene | CAS号201230-82-2 carbon monoxide | CAS号109-73-9 正丁胺 | CAS号2038-24-6 N-Butyl-1-propa... | CAS号855339-41-2 benzyl-butyl-pr... | CAS号2955-67-1 N-丁基丙酰胺 | CAS号107-10-8 丙胺 | CAS号123-72-8 正丁醛 | CAS号110-91-8 吗啉 | CAS号25413-64-3 N-butyl-N-propy...

合成工艺路线路线简述

    📜N-Propyliden-Butylamin置于二氢吡啶,Silica Gel体系中,用 苯 用作溶剂,化学反应 3.0H,以68%的收率获得n-丙基丁胺
    参考文献:Nad(P)+-nad(P)H 模型 70. 在硅胶存在下用 Hantzsch 酯还原亚胺
    标题:Nad(P)+-nad(P)H 模型 70. 在硅胶存在下用 Hantzsch 酯还原亚胺
    摘要:在硅胶存在下,亚胺被 Hantzsch 酯以高产率还原成相应的胺.还原显示出高化学选择性和立体选择性.α,β-不饱和亚胺的还原以高区域选择性进行以产生烯丙胺(1,2-还原产物).
    Doi:10.1246/bcsj.62.3845

    海关参考信息

    专利信息


    专利号:US-9738647-B2
    优先权日:2009-12-24
    标题:Methods for the synthesis of polycyclic guanidine compounds
    发明人:GRIDNEV ALEXEI
    权利人:NOVOMER INC; SAUDI ARAMCO TECH CO
    摘要:The present invention provides methods for the synthesis of polycyclic guanidine compounds. In certain embodiments, provided methods include the step of contacting a described reagent with a triamine compound to provide a polycyclic guanidine compound.

    专利号:US-4231955-A
    优先权日:1979-07-13
    标题 :Synthesis of alkyl and alkylaminonitriles
    发明人:CHANG CLARENCE D; LANG WILLIAM H; LAPIERRE RENE B
    权利人:MOBIL OIL CORP
    摘要:A method is provided for synthesizing alkylnitriles and alkylaminonitriles by reacting formaldehyde, a C1-C5 monohydric alcohol and a compound having the formula R1R2NH where R1 and R2 are selected from the group consisting of hydrogen and alkyl groups containing 1 to 5 carbon atoms under effective conditions in the presence of a catalyst comprising a crystalline aluminosilicate zeolite having a silica to alumina ratio of at least about 12 and a constraint index within the approximate range of 1 to 12 and recovering from the resulting reaction mixture, a product containing at least one of the above nitrile compounds.

    专利号:US-7741487-B2
    优先权日:2004-08-26
    标题 :Method for producing quaterrylene-3,4:13, 14-tetracarboxy diimides by direct synthesis
    发明人:KOENEMANN MARTIN; BOEHM ARNO; BIDLINGMAIER HERMANN; RIEGER REINHOLD; BLASCHKA PETER; REICHELT HELMUT; KRIEGER MATTHIAS
    权利人:BASF AG
    摘要:A process for preparing quaterrylene-3,4:13,14-tetracarboximides of the general formula I n nin whichn nR, R′ are each independently hydrogen or optionally substituted C 1 -C 30 -alkyl, C 5 -C 8 -cycloalkyl or aryl or hetaryl;n nwhich comprises reacting a perylene-3,4-dicarboximide of the general formula IIan n nin the presence of a base-stable, high-boiling, organic solvent and of an alkali metal base or alkaline earth metal base, with a perylene-3,4-dicarboximide of the general formula IIbn n nin which X is hydrogen, bromine or chlorine.

    专利号:US-7375058-B2
    优先权日:2001-09-14
    标 题:Herbicidal mixtures based on 3-phenyluracils
    发明人:ZAGAR CYRILL; SIEVERNICH BERND; QUAKENBUSH LAURA; EVANS RICHARD R; LANDES MAX; NEWSOM LARRY J; ORTLIP CHARLES L; WITSCHEL MATTHIAS; LANDES ANDREAS
    权利人:BASF AG
    摘要:Herbidically active compositions, comprising: A) at least one phenyluracil compound of the formula (I); in which the variables R 1 -R 7 are as defined in the claims, and/or at least one of its agriculturally acceptable salts; and at least one further active compound, selected from B) herbicides of classes b1) to b15): b1) lipid biosynthesis inhibitors; b2) acetolactate synthase inhibitors (ALS inhibitors); b3) photosynthesis inhibitors; b4) protoporphyrinogen-IX oxidase inhibitors; b5) bleacher herbicides; b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSP inhibitors); b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors); b9) mitose inhibitors; b10) inhibitors of the synthesis of very long chain fatty acids (VLCFA inhibitors); b11) cellulose biosynthesis inhibitors; b12) decoupler herbicides; b13) auxin herbicides; b14) auxin transport inhibitors; b15) other herbicides selected from the group consisting of benzoylprop, flamprop, flamprop-M, bromobutide, chlorflurenol, cinmethylin, methyldymron, etobenzanid, fosamine, metam, pyributicarb, oxaziclomefone, dazomet, triaziflam and methyl bromide; and safeners selected from: benoxacor, cloquintocet, cyometrinil, dichlormid, dicyclonon, dietholate, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, mephenate, naplithalic anhydride, 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine, 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane and oxabetrinil, the agriculturally acceptable salts of the active compounds B and C and the agriculturally acceptable derivatives of the active compounds B and C, provided they have a carboxyl group

    专利号:WO-2006079916-A1
    优先权日:2005-01-26
    标 题 :Thieno [2,3-d] pyrimidine compounds as inhibitors of adp-mediated platelets aggregation
    发明人:ENNIS MICHAEL DALTON; KORTUM STEVEN WADE; RAHMAN HAYAT; SCHWEITZER BARBARA ANN; TENBRINK RUTH ELIZABETH
    权利人:PHARMACIA & UPJOHN CO LLC; ENNIS MICHAEL DALTON; KORTUM STEVEN WADE; RAHMAN HAYAT; SCHWEITZER BARBARA ANN; TENBRINK RUTH ELIZABETH
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula (I): wherein A1, A2, A3, A4, A5, A6, A7, A8, X4, X6, R2, R4, R5, and R6 are as defined in the detailed description of the invention. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

    专利号:US-2014194622-A1
    优先权日:2009-12-24
    标 题 :Methods for the synthesis of polycyclic guanidine compounds

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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:Ishikawa, T., Science of Synthesis Knowledge Updates, (2012) 2, 333.
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