CAS: 6027-42-5; 1-Deoxy-1-Nitro-L-Mannitol

该化合物是一种属于糖酒精类的化学化合物,特别是马尼诺醇的衍生物,其特点是在第一个碳位置存在硝基化合物组(-NO2),该组与它的母化合物Manniotol有区别.这一改变会影响它的回旋性和生物特性.该化合物通常是白色晶体固,水中可溶解,并表现出血色色行为.其结构允许它参与各种化学反应,使其对有机合成感兴趣,并有可能对药用化学产生兴趣.该硝基化合物的存在可能会产生独特的特性,例如改变的相形色学或增强的生物活动.与许多硝基化合物一样,必须处理1-deoxy-1-nitro-L-mannitool,同时注意潜在的毒性和再活性.

结构式图片

MSDS等安全信息

上下游产品

nitromethane L-arabinose L-arabinose 1,2:5,6-di-O-isopropylidene-α-L-glucofuranose C-(α-L-arabinopyranosyl)nitromethane

合成工艺路线路线简述

    📜L-阿拉伯糖,硝基甲烷 反应生成 1-脱氧-1-硝基-L-甘露醇
    参考文献:Kopf,Jurgen;Brandenburg,Heinz;Seelhorst,Willy;Koll,Peter,Carbohydr. Res.,200,(1990) C. 339-354
    标题:Kopf,Jurgen;Brandenburg,Heinz;Seelhorst,Willy;Koll,Peter,Carbohydr. Res.,200,(1990) C. 339-354

    海关参考信息

    专利信息


    专利号:US-4207413-A
    优先权日:1977-04-22
    标 题 :L-Sucrose and process for producing same
    发明人:JONES JOHN K N; SZAREK WALTER A
    权利人:QUEEN S UNIV
    摘要:L-sucrose or beta -L-fructofuranosyl alpha -L-glucopyranoside-(I), the enantiomer of naturally occuring D-sucrose, which does not appear in nature has been synthesized and has been found to be sweet. It is unlikely that L-sucrose is metabolized in the manner of D-sucrose. In a preferred process for producing L-sucrose the key step is the condensation of 2,3,4,6-tetra-O-benzyl- alpha -L-glucopyranosyl chloride-(II) with 1,3,4,6-tetra-O-benzyl-L-fructofuranose-(III). Compound II is obtained from L-glucose by way of 2,3,4,6-tetra-O-benzyl- alpha -L-glucopyranose; and L-glucose is prepared from L-arabinose by nitromethane synthesis. Compound III is obtained by oxidation, with Jones reagent, of 1,3,4,6-tetra-O-benzyl-L-mannitol which, in turn, is prepared from L-mannose. The condensation product of II and III is catalytically debenzylated to produce L-sucrose.

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    品牌试剂参考报价(招募中)

    📌 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:Łaźny, R., Science of Synthesis, (2006) 8, 1251.
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