CAS: 60142-89-4; 7-((Tert-Butoxycarbonyl)Amino)Heptanoic Acid

该化合物是一种受保护的氨基酸衍生物,由N-终点的一个Boc(异丁氧碳基)组和C-终点的一个碳酸酯组组成,该化合物是peptide合成的多用途建筑块,特别是用于在生物凝聚和药物设计中引进空间武器或连接器.Boc组在基本条件下保持稳定,可以在酸性条件下有选择地予以保护,允许有控制的改变.它的七碳链提供了灵活性和水性疏漏,有助于裁缝分子特性.该化合物通常用于医药化学和材料科学,以进行可靠的再活动,并与标准的混合剂兼容.

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127582-76-7 929-17-9 62643-56-5

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CAS号24424-99-5 二碳酸二叔丁酯 | CAS号929-17-9 7-氨基庚酸 | CAS号116437-30-0 1-(tert-butoxyc... | CAS号6627-89-0 叔丁基苯基碳酸酯 | CAS号142356-34-1 (7-溴庚基)氨基甲酸叔丁酯 | CAS号19243-04-0 7-氨基-1-庚醇 | CAS号39979-08-3 7-氨基庚酸甲酯

合成工艺路线路线简述

    叔-丁基氯甲酸酯置于正丁基锂,Lithium Hydroxide Monohydrate体系中,用 四氢呋喃,水 作为反应溶剂,化学反应 4.67H,反应生成 7-(N-叔丁氧羰基氨基)庚酸
    参考文献:叔酰胺,仲酰胺和n-甲氧基酰胺的化学选择性还原亲核加成
    标题:叔酰胺,仲酰胺和n-甲氧基酰胺的化学选择性还原亲核加成
    摘要:随着目标分子在现代有机合成中的复杂性增加,化学选择性被认为是开发新方法的重要因素.酰胺羰基中心的化学选择性亲核加成是一个挑战,因为经典方法需要苛刻的反应条件以克服酰胺羰基的不良亲电性.我们已经成功开发出使用schwartz试剂将温和的亲核试剂还原性添加到叔酰胺,仲酰胺和n-甲氧基酰胺上的亲核试剂[cp 2Zrhcl].该反应在各种敏感的官能团,例如甲酯的存在下,以高度化学选择性的方式发生,这些官能团通常需要在亲核加成之前进行保护.该反应将适用于由容易获得的酰胺基团简单合成复杂的天然生物碱.
    DOI:10.1002/chem.201404648

    海关参考信息

    专利信息


    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

    专利号:US-5783577-A
    优先权日:1995-09-15
    标题 :Synthesis of quinazolinone libraries and derivatives thereof
    发明人:HOUGHTEN RICHARD A; OSTRESH JOHN M
    权利人:TREGA BIOSCIENCES INC
    摘要:The present invention provides synthetic combinatorial libraries of organic compounds based on the quinazolinone ring.

    专利号:WO-9710221-A1
    优先权日:1995-09-15
    标 题:Synthesis of quinazolinone libraries
    发明人:HOUGHTEN RICHARD A; OSTRESH JOHN M
    权利人:TORREY PINES INST
    摘要:The present invention provides synthetic combinatorial libraries of organic compounds based on the quinazolinone ring.

    专利号:US-2023295613-A1
    优先权日:2020-02-14
    标 题:Long chain carbon and cyclic amino acids substrates for genetic code reprogramming
    发明人:JEWETT MICHAEL C; LEE JOONGOO; MOORE JEFFREY S; SCHWARZ KEVIN J
    权利人:UNIV NORTHWESTERN; UNIV ILLINOIS
    摘要:Abstract: Disclosed are methods, systems, components, and compositions for synthesis of sequence defined polymers. The methods, systems, components, and compositions may be utilized for incorporating novel substrates that include non-standard amino acid monomers and non-amino acid monomers into sequence defined polymers. As disclosed herein, the novel substrates may be utilized for acylation of tRNA via flexizyme catalyzed reactions. The tRNAs thus acylated with the novel substrates may be utilized in synthesis platforms for incorporating the novel substrates into a sequence defined polymer.

    专利号:US-11814621-B2
    优先权日:2018-06-01
    标题 :Expanding the chemical substrates for genetic code reprogramming
    发明人:JEWETT MICHAEL CHRISTOPHER; LEE JOONGOO; MOORE JEFFREY S; SCHWIETER KENNETH E; SCHWARZ KEVIN JEROME
    权利人:UNIV NORTHWESTERN; UNIV ILLINOIS
    摘要:Disclosed are methods, systems, components, and compositions for synthesis of sequence defined polymers. The methods, systems, components, and compositions may be utilized for incorporating novel substrates that include non-standard amino acid monomers and non-amino acid monomers into sequence defined polymers. As disclosed herein, the novel substrates may be utilized for acylation of tRNA via flexizyme catalyzed reactions. The tRNAs thus acylated with the novel substrates may be utilized in synthesis platforms for incorporating the novel substrates into a sequence defined polymer.

    专利号:US-8475998-B2
    优先权日:2010-12-20
    标 题 :Compound synthesis method, microarray, acid-transfer composition, and biochip composition
    发明人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI
    权利人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI; SAMSUNG ELECTRONICS CO LTD; JSR CORP
    摘要:A compound synthesis method includes bonding a first compound to a substrate to form a first film. A second film is formed on the first film using an acid-transfer composition including (A) a polymer that includes a structural unit shown by a following formula (1) and a structural unit shown by a following formula (2), (B) a photoacid generator shown by a following formula (3), and (C) a sensitizer shown by a following formula (4). The second film is exposed to remove the protecting group from the first compound under an exposed area of the second film. An acid generated in the exposed area of the second film is transferred to the first film. The second film after being exposed is removed. A second compound is bonded to the first compound from which the protecting group has been removed.
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    合成参考文献


    参考文献:10.1007/978-1-0716-1920-9_20
    摘要:Ohoka N, Yokoo H, Okuhira K, Demizu Y, Naito M. Molecular Design, Synthesis, and Evaluation of SNIPER (ER) that Induces Targeted Protein Degradation of ERα. Methods Mol Biol. 2022;2418():363–82. doi: 10.1007/978-1-0716-1920-9_20.
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