CAS: 35161-70-7; N-Methylhexan-1-Amine

该化合物是被归类为丙烯的有机化合物,一般看起来无色的黄色液体,具有典型的矿泉味;该化合物以分子重量相对较低和中度沸点闻名,因此是一种挥发性物质.甲基丙基胺在有机溶剂中可溶解,但由于其盐分碳基链,其溶解性在水中有限,主要用于各种工业用途,包括作为合成药物,农用化学品和其他有机化合物的建筑块.此外,该化合物在某些配方中可作为表面活性剂或凝聚抑制剂.甲基丙基胺可以表现出基本特性,与酸一起形成盐状.在处理该化合物时,安全因素十分重要,因为它可能会刺激皮肤,眼睛和呼吸系统.建议使用适当的保护设备和通风设备来减轻潜在的健康风险.

结构式图片

相似化合物

2439-54-5 7311-30-0 36343-05-2

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ECHA物质C&L通报REACH预注册

上下游产品

CAS号111-26-2 正己胺 | CAS号100-61-8 N-甲基苯胺 | CAS号2591-78-8 Formamide,N-hexyl | CAS号1072-44-2 Methylaziridine, 1 | CAS号111-25-1 1-溴代正己烷 | CAS号74-89-5 氨基甲烷 | CAS号62316-77-2 N-diphenylphosp... | CAS号62316-73-8 N-diphenylphosp... | CAS号66-25-1 正己醛 | CAS号544-10-5 氯(代)正己烷 | CAS号4385-04-0 N,N-二甲基己胺 | CAS号37615-53-5 N-甲基二己胺 | CAS号69-72-7 水杨酸 | CAS号6378-65-0 己酸己酯 | CAS号25468-44-4 N-苄基-N-己基胺

合成工艺路线路线简述

    N-己基甲酰胺置于氢气体系中,用 乙二醇二甲醚 作为反应溶剂,160.0 °C,3.0 Mpa 条件下,反应 20.0H,反应生成 N-己基甲胺
    参考文献:在温和条件下将酰胺催化加氢为胺
    标题:在温和条件下将酰胺催化加氢为胺
    摘要:在(不是很大)压力下:已开发出一种使用双金属pd-Re催化剂将叔酰胺和仲酰胺氢化成胺的通用方法,具有优异的选择性.反应在低压和较低温度下进行.该方法为有机化学家提供了一种简单可靠的胺合成工具.
    DOI:10.1002/anie.201207803

    海关参考信息

    专利信息


    专利号:US-2005130201-A1
    优先权日:2003-10-14
    标 题 :Splint-assisted enzymatic synthesis of polyribounucleotides
    发明人:DERAS MICHAEL; PLEISS JEFFREY A; SCARINGE STEPHEN
    权利人:DHARMACON INC
    摘要:The present invention comprises methods and compositions for splint-assisted enzymatic synthesis of polyribonucleotides using an RNA polymerizing enzyme. The invention provides ligating ribonucleotides comprising ligating a donor RNA molecule to an acceptor RNA molecule in the presence of RNA ligase and a splint, wherein the donor RNA molecule is comprised of at least one nucleotide and a ligation linker moiety, the acceptor RNA molecule is comprised of at least one nucleotide and a ligation linker moiety and the splint is comprised of a polyribonucleotide. The invention also provides splints for use in splint-assisted enzymatic synthesis using an RNA polymerizing enzyme.

    专利号:US-5484949-A
    优先权日:1993-01-29
    标题:Method for the synthesis of α β-unsaturated ketones
    发明人:TSUKASHIMA KEIICHI; NAKAJIMA MASASHI; FUJIMARU MASAYOSHI; SUZUKI KENJI
    权利人:NIPPON SODA CO
    摘要:The present invention relates to a method for the synthesis of alpha , beta -unsaturated ketones which comprises, in the method for the synthesis of alpha , beta -unsaturated ketones represented by general formula reacting aldehydes represented by general formula R1CHO (where R1 is as defined above) with alkali metal salt of acetoacetic acid represented by general formula sence as a catalyst of 3-azabicyclo[3,2,2]nonane, a cyclic secondary amine represented by general formula (1) (1) a cyclic secondary amine represented by general formula (2) (2) (where, l is 1 or more and up to 6, a ring with N is a 6-membered, 7-membered or 8-membered ring, the two neighbors of N are methylene, R3 is a lower alkyl group, its substitution position is at a carbon atom other than two those adjacent to N, and is an alicyclic group or a phenol group), or a secondary amine represented by general formula (3) CH3NHCH2R4(3) in a mixuture solvent of water and water-insoluble organic solvent, while keeping the pH constant with mineral acid, and by adjusting an amount of water.

    专利号:US-6765117-B2
    优先权日:1997-10-24
    标题:Process for stereoselective synthesis of prostacyclin derivatives
    发明人:MORIARTY ROBERT M; PENMASTA RAJU; GUO LIANG; RAO MUNAGALA S; STASZEWSKI JAMES P
    权利人:UNITED THERAPEUTIC CORP
    摘要:An improved method is described for making 9-deoxy-PGF 1 -type compounds. In contrast to the prior art, the method is stereoselective and requires fewer steps than the known methods for making these compounds. The invention also relates to novel intermediates prepared during the synthesis of the 9-deoxy-PGF 1 -type compounds.

    专利号:US-5043328-A
    优先权日:1986-05-09
    标 题 :Formulations containing unsaturated fatty acids for the synthesis of prostaglandins and hydroxy-fatty acids in biological systems
    发明人:WEITHMANN KLAUS U
    权利人:HOECHST AG
    摘要:The present invention relates to formulations containing unsaturated fatty acids for the synthesis of prostaglandins and hydroxy-fatty acids in biological systems and to the use of such formulations for the preparation of medicaments which are suitable for curing prostaglandin deficiencies in humans or animal, for example healing or preventing diseases of the gastro-intestinal tract.

    专利号:US-2008206850-A1
    优先权日:2007-02-28
    标 题:Methods and compositions for DNA synthesis
    发明人:DELLINGER DOUGLAS J; DELLINGER GERALDINE F; CARUTHERS MARVIN H
    权利人:DELLINGER DOUGLAS J; DELLINGER GERALDINE F; CARUTHERS MARVIN H
    摘要:In some embodiments, the present disclosure relates to new phosphoramidite compositions, that have Silyl-containing carbonate or thiocarbonate or ether as 5′-hydroxyl protecting groups useful of the synthesis of DNA, and in particular for the synthesis of long sequences of DNA (e.g., >50 mer). In some embodiments, there are provided methods for simultaneous oxidation of the internucleoside phosphate triester linkages and removal of the 5′-hydroxyl-protecting group, making this process a new 2-step DNA synthesis, that involves the use of peroxyanions in combination with fluoride anions.

    专利号:US-2008206851-A1
    优先权日:2007-02-28
    标题:Methods and compositions for RNA synthesis
    发明人:DELLINGER DOUGLAS J; DELLINGER GERALDINE F; CARUTHERS MARVIN H
    权利人:DELLINGER DOUGLAS J; DELLINGER GERALDINE F; CARUTHERS MARVIN H
    摘要:In some embodiments, the present disclosure relates to new phosphoramidite compositions, that have Silyl-containing carbonate or thiocarbonate or ether as 5′-hydroxyl protecting groups useful fo the syntheis of RNA, and in particular for the synthesis of long sequences of RNA (e.g., >50 mer). In some embodiments, there are provided methods for simultaneous oxidation of the internucleoside phosphate triester linkages and removal of the 5′-hydroxyl-protecting group, making this process a new 2-step RNA synthesis, that involves the use of peroxyanions in combination with fluoride anions.
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    主要参考文献

    [参考文献]: Masaru Utsunomiya, Et Al. Ruthenium-Catalyzed Anti-Markovnikov Hydroamination Of Vinylarenes. J Am Chem Soc. 2004 Mar 10;126(9):2702-3.

    合成参考文献


    摘要:Ipaktschi, J.; Saidi, M. R., Science of Synthesis Knowledge Updates, (2012) 4, 446.
    摘要:Scholz, U.; Dong, W.; Feng, J.; Shi, W., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 68.
    摘要:Journal of Pharmacology and Experimental Therapeutics., 103(325), 1951 []
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