CAS: 69342-47-8; 4-N-Butylphenylisocyanate

该化合物是一种专门有机化合物,主要用作尿素,氨基甲酸盐和其他异氰酸盐衍生物合成的活性中间体,其化学结构以丁基苯为主,在聚合和交叉链接应用中增强活性和选择性,该化合物因其在受控条件下形成稳定的聚氨酯联系的能力而在涂层,粘合剂和弹性生产中特别具有价值,在普通有机溶剂中表现出良好的溶解性,便于将其纳入各种配方.适当处理至关重要,因为它对水具有敏感性,需要在惰性条件下储存以防止过早聚合.其持续的纯度和再活性使得它成为工业和研究应用的可靠选择.

结构式图片

欧盟法规

ECHA物质C&L通报

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CAS号104-13-2 4-正丁基苯胺 | CAS号32315-10-9 三光气 | CAS号13478-63-2 4-butylaniliniu... | CAS号86764-31-0 1,1-dibenzyl-3-... | CAS号86781-18-2 1,1-dibutyl-3-(...

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    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-2005192265-A1
    优先权日:2003-03-20
    标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting beta-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J
    摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:US-6906056-B2
    优先权日:1998-06-22
    标 题:Cycloalkyl, lactam, lactone and related compounds, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
    发明人:THOMPSON RICHARD C; WILKIE STEPHEN; STACK DOUGLAS R; VANMETER ELDON E; SHI QING; BRITTON THOMAS C; AUDIA JAMES E; REEL JON K; MABRY THOMAS E; DRESSMAN BRUCE A; CWI CYNTHIA L; HENRY STEVEN S; MCDANIEL STACEY L; STUCKY RUSSELL D; PORTER WARREN J
    权利人:LILLY CO ELI
    摘要:Disclosed are compounds which inhibit β-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer's disease. Also disclosed are pharmaceutical compositions that include a compound which inhibits β-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer's disease both prophylactically and therapeutically with such pharmaceutical compositions.

    专利号:CN-116137864-A
    优先权日:2020-07-23
    标 题:Synthesis of linear polyoxazolidinones using uretdiones as diisocyanate component

    专利号:CN-111471171-B
    优先权日:2019-01-24
    标 题:A kind of aryl sulfonic acid intermediate and its preparation method, and its application for the synthesis of low temperature sensitive admixture for concrete

    专利号:US-2011015119-A1
    优先权日:2009-06-24
    标题:Novel semi-synthetic glycopeptides as antibacterial agents
    发明人:CHU DANIEL; YE TAO; WANG BING
    权利人:LEAD THERAPEUTICS INC
    摘要:Semi-synthetic glycopeptides having antibacterial activity are described, in particular, the semi-synthetic glycopeptides described herein are made by chemical modification of a glycopeptide (Compound A, Compound B, Compound H or Compound C) or monosaccharide made by hydrolyzing the disaccharide moiety of the amino acid-4 of the parent glycopeptide in acidic medium to give the amino acid-4 monosaccharide; conversion of the monosaccharide to the amino-sugar derivative; acylation of the amino substituent on the amino acid-4 amino-substituted sugar moiety on these scaffolds with certain acyl groups; and conversion of the acid moiety on the macrocyclic ring of these scaffolds to certain substituted amides. Key reaction is the treatment of properly protected intermediate compound with isocyanate. Also provided are methods for the synthesis of the compounds, pharmaceutical compositions containing the compounds, and methods of use of the compounds for the treatment and/or prophylaxis of diseases, especially bacterial infections.
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    合成参考文献


    摘要:Braverman, S.; Cherkinsky, M., Science of Synthesis Knowledge Updates, (2014) 3, 259.
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