4,6-Dideoxy-4-[(2-methoxypropanoyl)amino]-3-C-methyl-2-O-methyl-L-mannose is a complex carbohydrate derivative with specific structural features that contribute to its chemical properties. This compound is characterized by the presence of multiple functional groups, including a methoxypropanoyl moiety and methyl groups, which influence its solubility and reactivity. The presence of dideoxy and C-methyl groups indicates modifications that can affect its biological activity and interaction with enzymes or receptors. As a derivative of L-mannose, it retains some of the properties of monosaccharides, such as potential involvement in glycosylation processes. The compound's unique structure may also suggest potential applications in medicinal chemistry, particularly in the development of glycosylated drugs or as a probe in biochemical research. Its CAS number, 92355-88-9, allows for easy identification in chemical databases, facilitating research and development efforts. Overall, this compound exemplifies the complexity and diversity of carbohydrate chemistry, with implications for both synthetic and natural product chemistry.

N-Acylkansosamine is a N-acylamino sugar from trehalose-containing lipopolysaccharide antigens of Mycobacterium kansasii.

4,6-dideoxy-4-[(2-methoxypropanoyl)amino]-3-C-methyl-2-O-methyl-L-mannose

92355-88-9: 4,6-Dideoxy-4-[(2-methoxypropanoyl)amino]-3-C-methyl-2-O-methyl-L-mannose is a complex carbohydrate derivative with specific structural features that contribute to its chemical properties. This compound is characterized by the presence of multiple functional groups, including a methoxypropanoyl moiety and methyl groups, which influence its solubility and reactivity. The presence of dideoxy and C-methyl groups indicates modifications that can affect its biological activity and interaction with enzymes or receptors. As a derivative of L-mannose, it retains some of the properties of monosaccharides, such as potential involvement in glycosylation processes. The compound's unique structure may also suggest potential applications in medicinal chemistry, particularly in the development of glycosylated drugs or as a probe in biochemical research. Its CAS number, 92355-88-9, allows for easy identification in chemical databases, facilitating research and development efforts. Overall, this compound exemplifies the complexity and diversity of carbohydrate chemistry, with implications for both synthetic and natural product chemistry.

N-Acylkansosamine is a N-acylamino sugar isolated from trehalose-containing lipopolysaccharide antigens of Mycobacterium kansasii.

CAS 92355-88-9

4,6-dideoxy-4-[(2-methoxypropanoyl)amino]-3-C-methyl-2-O-methyl-L-mannose

N-Acylkansosamine

Ref: TM-T25846