Acylaminobenzoic acid and derivatives
Medchemexpress LLC 4-acetamido-5-chloro-2-methoxybenzoic acid | 24201-13-6 | MFCD07783714 | 99.4% | 243.65 g/mol | C10H10ClNO4 | 500 MG
4-Acetamido-5-chloro-2-methoxybenzoic acid is a chemical intermediate used in pharmaceutical research and synthesis; it is also identified as Metoclopramide Impurity 12 and is supplied as a white to off-white solid suitable for medicinal chemistry applications.
- High purity: 99.4%.
- Molecular formula: C10H10ClNO4; molecular weight: 243.65 g/mol.
- Appearance: white to off-white solid.
- Storage: powder at -20°C (up to 3 years) or 4°C (up to 2 years); in solvent at -80°C (6 months) or -20°C (1 month).
- Packaging: available in sizes from 100 mg to 10 g.
Medchemexpress LLC Chloro-2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose | 3068-34-6 | 98.0% | 365.76 | 500 MG
Chloro 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranose is a biochemical reagent used in glycobiology research. Glycobiology involves the study of the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is relevant to basic research, biomedicine, and biotechnology.
- Used in glycobiology research.
- Relevant to carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems.
- Closely related to basic research, biomedicine, and biotechnology.
- Available with a purity of 98.0%.
Medchemexpress LLC 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl chloride | 41355-44-6 | MFCD00047513 | >98.0% | 365.76 g/mol | C14H20ClNO8 | 500 MG
2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl chloride is an acetyl-protected glycosyl chloride used as a glycosyl donor and synthetic intermediate in carbohydrate chemistry and glycobiology research. It is employed to assemble oligosaccharides and glycan analogues via glycosylation reactions and is handled under standard laboratory safety procedures.
- Acetyl-protected glycosyl donor suitable for glycosylation reactions.
- Facilitates synthesis of oligosaccharides and glycan analogues.
- Reactive anomeric chloride enables coupling under standard activation conditions.
- Compatible with common protecting group strategies in carbohydrate synthesis.
- Supplied for research use; handle with appropriate PPE and protocols.