CAS: 172945-26-5; β-D-Glucopyranoside, Hexyl 2-(Acetylamino)-2-Deoxy-, 3,4,6-Triacetate

该化合物是D-甘蔗糖合成胶合胶层衍生物,其特点是存在一个乙基氨基氨组和一个丙基链;该化合物的特点是一个六人环球甘蓝糖结构,由六人组成的循环甘蓝组成,其中三组乙基乙基,附于第3,4,6号阵地的氢氧基,加强了其亲脂性和稳定性;该乙基基酰组促成其疏水特性,使其有可能用于各种生物化学应用,包括药物运载系统和表面活性剂;氢氧组的乙基可影响化合物的溶性和再活性,使之适合生物系统中的特定化学反应或相互作用;其化学文摘社编号172945-26-5,允许在化学数据库中准确识别.总体而言,该化合物体现了有机化学和生物化学中甘油表面的结构复杂性和功能多变性.

结构式图片

相似化合物

190912-49-3 211567-22-5 173725-22-9

MSDS等安全信息

    上下游产品

    2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline hexan-1-ol Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl diphenylphosphinatehexyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside Hexyl 2-acetamido-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside propoxymethyl>-β-D-glucopyranosideHexyl 2-acetamido-3-O-benzoyl-6-O-benzyl-2-deoxy-4-O-3-(methyl 4,7,8,9-tetra-O-acetyl-N-acetyl-α-D-neuraminate-2-yl)oxypropoxymethyl-β-D-glucopyranoside Hexyl 2-acetamido-6-O-benzyl-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-2-deoxy-β-D-glucopyranoside

    合成工艺路线路线简述

    • 合成目标产物 Hexyl 2-Acetamido-3,4,6-Tri-O-Acetyl-2-Deoxy-Beta-D-Glucopyranoside 主要起始原料 2-Acetamido-2-Deoxy-Alpha-D-Glucopyranosyl Chloride 3,4,6-Triacetate And 1-Hexanol
    • (文献来源)合成步骤主要原料 2-Acetamido-2-Deoxy-Alpha-D-Glucopyranosyl Chloride 3,4,6-Triacetate 和 1-Hexanol
    📜2-Deoxy-2-Acetamido-3,4,6-Tri-O-Acetyl-D-Glucopyranose置于1H-1,2,4-三唑,三氟甲磺酸三甲基硅酯,双氧水体系中,用 硝基甲烷,二氯甲烷 用作溶剂,化学反应 15.0H,反应生成己基-2,3,4,6-四-氧-乙酰基-β-D-吡喃葡萄糖苷
    参考文献:New α-Selective Thermal Glycosylation Of Acetyl-Protected 2-Acetamido-2-Deoxy-β-D-Glucopyranosyl Diphenylphosphinate
    标题:New α-Selective Thermal Glycosylation Of Acetyl-Protected 2-Acetamido-2-Deoxy-β-D-Glucopyranosyl Diphenylphosphinate
    摘要:This Paper Describes New Alpha-Selective Thermal Glycosylation Using Acetyl-Protected 2-Acetamido-2-Deoxy-Beta-D-Glucopyranosyl Diphenylphosphinate (4) As A Glycosyl Donor. When The Glycosylation Of 4 With 1-Hexanol Was Carried Out Under Various Conditions,The Conditions Using Trimethylsilyl Trifluoromethanesulfonate As A Promoter In Nitromethane At Reflux Temperature Were Most Suitable For The Formation Of The Alpha Anomer. The Glycosylation Of 4 With The Other Common Alcohols Gave Corresponding Alpha-Glycosides In Relatively High Yields Under The Conditions. When Cholesterol,A Very Steric Hindered Alcohol,Was Used As A Glycosyl Acceptor,Alpha-Glycoside Was Also Produced Predominantly. (C) 2000 Elsevier Science Ltd. All Rights Reserved.
    Doi:10.1016/s0008-6215(00)00069-0

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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:10.1016/S0008-6215(99)00030-0
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