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6-Deoxy-alpha-L-galactopyranosyl-(1->4)-[6-deoxy-alpha-L-galactopyranosyl-(1->2)-beta-D-galactopyranosyl-(1->3)]-2-acetamido-2-deoxy-beta-D-glucopyranosyl-(1->3)-beta-D-galactopyranosyl-(1->4)-D-gluco se(CAS: 16789-38-1)
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CAS号
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基本信息
分子式
C38H65NO29
分子量
999.92 g/mol
Physical Properties
沸点
1349.9±65.0 °C(Predicted)
密度
1.71±0.1 g/cm3(Predicted)
化学标识符
SMILES
C[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H](O[C@H]([C@@H]([C@H]2O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O)O[C@H]4[C@H]([C@@H]([C@@H]([C@@H](O4)C)O)O)O)NC(=O)C)O[C@H]5[C@H]([C@H](O[C@H]([C@@H]5O)O[C@H]([C@@H](CO)O)[C@@H]([C@H](C=O)O)O)CO)O)CO)O)O)O
InChIKey
OQIUPKPUOLIHHS-URTONSIPSA-N
数据库引用
MDL号
MFCD00792848
常见问题
LACTO-N-DIFUCOHEXAOSE I 乳糖-N-二岩藻六糖 I为白色结晶性粉末，分子量约为1036.25。该化合物不溶于水，但易溶于乙醇、丙酮等有机溶剂。它具有复杂的糖苷结构，显示出一定的反应活性，特别是在糖苷键的水解和衍生化反应中表现出较高的活性。
LACTO-N-DIFUCOHEXAOSE I 乳糖-N-二岩藻六糖 I通常通过多步糖苷合成反应制备，包括糖苷键的形成和后期修饰。常用的合成方法包括酶促合成和化学合成。在酶促合成中，通常使用特定的糖苷酶催化反应，而在化学合成中，可以使用醇解、缩合等反应来构建糖苷骨架，并通过后期化学修饰实现目标化合物的合成。
LACTO-N-DIFUCOHEXAOSE I 乳糖-N-二岩藻六糖 I主要应用于医药行业，作为糖类药物或保健品的中间体。在聚合物领域，它可以作为合成特殊聚合物的单体。此外，在传感器和半导体领域，该化合物也可作为研究对象，探索其在特定功能材料中的应用潜力。
在处理LACTO-N-DIFUCOHEXAOSE I 乳糖-N-二岩藻六糖 I时，实验室应保持良好的通风，操作应在通风橱中进行。佩戴适当的个人防护装备（PPE），如手套、护目镜等。避免与皮肤和眼睛直接接触，若不慎接触，应立即用大量清水冲洗。储存时应远离火源和热源，保持容器密封。参考安全数据表（SDS）获取完整安全信息。
安全须知
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