CAS: 3320-87-4; 3-Nitrophenylisocyanate

该化合物是一种活性有机化合物,主要用作化学合成的多功能中间体.它的关键功能组,即异氰酸盐混合物,能够对氨和酒精等核素产生有效反应,使其对生产尿素,氨基甲酸盐和其他衍生物具有价值.处于元值的硝基化合物组增强了其反应性,在电动芳香替代反应中起到了作用.该化合物在制药,农用化学品和聚合物研究中特别有用,因为它能够将硝基苯功能引入目标分子中.它通常在受控制的条件下处理,因为它的湿度敏感度和潜在的刺激性.建议在无水环境中适当储存以保持稳定性.

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ECHA物质ECHA物质C&L通报REACH预注册

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CAS号32315-10-9 三光气 | CAS号99-09-2 间硝基苯胺 | CAS号99-65-0 间二硝基苯 | CAS号201230-82-2 carbon monoxide | CAS号51028-37-6 (3-nitrophenyl)... | CAS号33322-43-9 3-nitro-benzoic... | CAS号503-38-8 氯甲酸三氯甲酯 | CAS号121-92-6 间硝基苯甲酸 | CAS号33240-96-9 3-硝基苯胺盐酸盐 | CAS号29639-03-0 (3-nitro-phenyl... | CAS号3529-82-6 3-硝基异硫氰酸苯酯 | CAS号2000-54-6 Urea,N-(3-nitro... | CAS号18437-64-4 叔丁基(3-硝基苯基)氨基甲酸酯 | CAS号1234-21-5 Urea,N,N'-bis(3... | CAS号93-97-0 苯甲酸酐 | CAS号2610-62-0 Carbamic acid,(... | CAS号68621-88-5 N-B°C-间苯二胺 | CAS号13142-61-5 1-(3-硝基苯基)脲 | CAS号13208-56-5 1-(4-chlorophen... | CAS号101-22-4 N,N'-bis(3-amin...

合成工艺路线路线简述

    📜3-硝基异硫氰酸苯酯置于sodium Hydride体系中,用 5,5-Dimethyl-1,3-Cyclohexadiene,氯仿,乙腈,Mineral Oil 作为反应溶剂,化学反应 3.0H,反应生成 3-硝基苯异氢酸酯
    参考文献:硫从1,2,4-二噻唑烷-3,5-二酮向三苯膦转移的机理
    标题:硫从1,2,4-二噻唑烷-3,5-二酮向三苯膦转移的机理
    摘要:研究了在25oc下用4-(3-和4-取代)-1,2,4-二噻唑烷-3,5-二酮在乙腈,二氯甲烷,四氢呋喃和甲苯中取代的三苯基膦的硫化机理.反应途径包括限制磷对硫的最初亲核进攻,然后将intermediate中间体快速分解为相应的膦硫化物,苯基异氰酸酯和羰基硫化物.从哈米特相关性和对溶剂的依赖性,可以得出结论,过渡态结构是非常极性的,类似于两性离子中间体.在溶剂系列中,Ps键形成和ss键断裂的程度非常相似,但是随着溶剂极性的降低,后者逐渐降低.版权所有©2013 John Wiley&sons,Ltd.
    DOI:10.1002/poc.3131

    海关参考信息

    专利信息


    专利号:US-4341898-A
    优先权日:1981-05-18
    标题:Synthesis of isocyanates from nitroalkanes
    发明人:MILLIGAN BARTON; PINSCHMIDT JR ROBERT K
    权利人:AIR PROD & CHEM
    摘要:A process for the preparation of aromatic isocyanates from nitroalkanes. A nitromethyl aromatic compound of the general formula: wherein R and R1 represent hydrogen, halogen, a C1-C5 alkyl radical, a C1-C4 alkoxy radical, nitro, isocyanato, an alkoxycarbonylamino, or nitromethyl radical, with R and R1 being the same or different, is heated in the presence of an effective amount of a Lewis acid or Bronsted acid substance to effect a dehydrogenation-isomerization reaction to yield an aromatic isocyanate of the general formula: The product of the reaction may be recovered as the aromatic isocyanate or the alcohol adduct, a carbamate.

    专利号:US-9833457-B2
    优先权日:2008-01-25
    标题:Tricyclic compounds as modulators of TNF-α synthesis and as PDE4 inhibitors
    发明人:MJALLI ADNAN M M; GADDAM BAPU; POLISETTI DHARMA RAO; KOSTURA MATTHEW J; GUZEL MUSTAFA
    权利人:VTV THERAPEUTICS LLC
    摘要:The present invention relates to chemical compounds of Formula (I) are as herein defined, pharmaceutical compositions, and methods of use in the treatment of conditions or disorders mediated by TNF-α or by PDE4, including but not limited to psoriatic arthritis.

    专利号:US-4158672-A
    优先权日:1976-01-26
    标题 :Polyfluoroalkylthio alcohols, esters and useful compositions therefrom
    发明人:DEAR ROBERT E A; BRACE NEAL O
    权利人:CIBA GEIGY CORP
    摘要:Polyfluoroalkylthio alcohols and esters thereof are disclosed with utility as intermediates for the synthesis of fluorochemicals with low free surface energies having oil and water repellent properties. The novel alcohols and esters are obtained by a free radical catalyzed addition of polyfluoroalkylthiols to acetylenic alcohols or esters thereof. The alcohols are employed in preparation of fluorine containing polyurethanes which are useful as finishes to provide oil and water repellency to textiles and as additives to plastics to provide mold release and other desirable properties.

    专利号:US-4001305-A
    优先权日:1974-02-04
    标 题:Rf-glycols containing two perfluoroalkylthio groups and useful compositions therefrom
    发明人:DEAR ROBERT ERNEST ARTHUR; FALK ROBERT ALLAN
    权利人:CIBA GEIGY CORP
    摘要:Perfluoroalkylthio glycols and esters thereof can be prepared by the free-radical catalyzed addition of a perfluoroalkylthiol to an acetylenic alcohol or ester thereof. The compounds obtained are useful intermediates for the synthesis of fluorochemicals with low free surface energies having oil and water repellent properties. In one embodiment, a perfluoroalkylthio glycol can be reacted with a diisocyanate to obtain a polyurethane containing perfluoroalkylthio groups, which polyurethanes are useful as coatings to provide oil and water repellence to textiles and as additives to plastics to provide mold-release and other desirable properties.

    专利号:US-4054592-A
    优先权日:1974-02-04
    标题 :Urethanes containing two perfluoroalkylthio groups
    发明人:DEAR ROBERT ERNEST ARTHUR; FALK ROBERT ALLAN
    权利人:CIBA GEIGY CORP
    摘要:Perfluoroalkylthio glycols and esters thereof can be prepared by the free-radical catalyzed addition of a perfluoroalkylthiol to an acetylenic alcohol or ester thereof. The compounds obtained are useful intermediates for the synthesis of fluorochemicals with low free surface energies having oil and water repellent properties. In one embodiment, a perfluoroalkylthio glycol can be reacted with a diisocyanate to obtain a polyurethane containing perfluoroalkylthio groups, which polyurethanes are useful as coatings to provide oil and water repellence to textiles and as additives to plastics to provide mold-release and other desirable properties.

    专利号:US-4097642-A
    优先权日:1975-11-12
    标题:Fabric coated with RF-glycols containing two perfluoroalkylthio groups
    发明人:DEAR ROBERT ERNEST ARTHUR; FALK ROBERT ALLAN
    权利人:CIBA GEIGY CORP
    摘要:Perfluoroalkylthio glycols and esters thereof can be prepared by the free-radical catalyzed addition of a perfluoroalkylthiol to an acetylenic alcohol or ester thereof. The compounds obtained are useful intermediates for the synthesis of fluorochemicals with low free surface energies having oil and water repellent properties. In one embodiment, a perfluoroalkylthio glycol can be reacted with a diisocyanate to obtain a polyurethane containing perfluoroalkylthio groups, which polyurethanes are useful as coatings to provide oil and water repellance to textiles and as additives to plastics to provide mold-release and other desirable properties.

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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:Braverman, S.; Cherkinsky, M.; Birsa, M. L., Science of Synthesis, (2005) 18, 140.
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