CAS: 130752-32-8; Fmoc-D-Arg-Oh

该化合物是一种受保护的氨酸D-arginine,通常用于peptide合成.Fmoc组是一种保护性动物,在合成过程中可以有选择性地取消保护.该组具有基本的侧链,因为它在正辛酸中存在促进极地溶剂溶解的,该组在表面上一般白色,在标准实验室条件下稳定.Fmoc-D-Arg-OH,它存在于二甲基二甲基二苯丙胺和二甲基硫氧化二甲基硫酸等有机溶剂中,但水中的溶解度较少.该化合物用于合成peptid和蛋白质,特别是在固相聚聚物合成中,在基本条件下可以很容易去除Fmoc组.在生物化学研究和药物开发中具有价值,在设计生物活性化学剂时,应作为所有化学剂的防范剂.

结构式图片

相似化合物

1119-34-2 114622-81-0 1159-15-5

上下游产品

Nα-(9-fluorenylmethoxycarbonyl)-Nγ-(4-methoxy-2,3,6-trimethylbenzenesulphonyl)-L-arginine α-9-Fluorenylmethyloxycarbonyl-NG-2,4,6-triisopropylbenzenesulphonyl-L-arginineNα-9-Fluorenylmethyloxycarbonyl-NG-2,4,6-triisopropylbenzenesulphonyl-L-arginine α-9-Fluorenylmethyloxycarbonyl-NG-4-methoxy-3,5-di-tert-butylbenzenesulphonyl-L-arginineNα-9-Fluorenylmethyloxycarbonyl-NG-4-methoxy-3,5-di-tert-butylbenzenesulphonyl-L-arginine α-9-fluorenylmethyloxycarbonyl-NG-biphenyl-4-sulphonyl-L-arginineNα-9-fluorenylmethyloxycarbonyl-NG-biphenyl-4-sulphonyl-L-arginine

合成工艺路线路线简述

    📜N'-[(2,3-二氢-2,2,4,6,7-五甲基苯并呋喃-5-基)磺酰基]-N-芴甲氧羰基-D-精氨酸置于三氟乙酸体系中,用 乙腈 用作溶剂,化学反应 0.33H,反应生成Fmoc-D-精氨酸
    参考文献:Pressurized Sample Infusion: An Easily Calibrated,Low Volume Pumping System For Esi-Ms Analysis Of Reactions
    标题:Pressurized Sample Infusion: An Easily Calibrated,Low Volume Pumping System For Esi-Ms Analysis Of Reactions
    摘要:Pressurized Sample Infusion (Psi) Continuously Delivers Solution From A Flask Through Capillary Tubing At A Flow Rate That Makes It Suitable As A Low Internal Volume Pumping Method For Electrospray Ionization Mass Spectrometry (Esi-Ms). The Flow Rate Can Be Predicted From The Applied Pressure By Using The Hagen-Poiseuille Equation,But Variability In Internal Diameter Of The Peek Tubing Used Is Such That Each Individual Length Should Be Calibrated If Accurate Results Are Sought. Once Calibrated,The Values Hold Well For Different Solvents Across A Range Of Pressures. The Technique Has Been Exemplified In Two Reactions: The Deprotection Of A Protected Amino Acid Using Trifluoroacetic Acid,And In The Platinum-Catalyzed Redistribution Of Two Silanes. In Both Cases,The Abundances Of Starting Material,Product(S) And Intermediates Were Tracked In Real Time As The Reaction Proceeded. (C) 2012 Elsevier B.V. All Rights Reserved.
    Doi:10.1016/j.Ijms.2012.03.007

    海关参考信息

    专利信息


    专利号:CN-112574285-B
    优先权日:2019-09-29
    标题 :A kind of solid-liquid phase synthesis method of polypeptide drug containing a pair of disulfide bonds

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    ✅ COA系统入驻 | 共享模式

    合成参考文献

    合成方法参考DOI号:10.1080/00397910802632563
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