Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside
Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside (CAS 54400-75-8), with the molecular formula C11H19NO6 and a molecular weight of 261.27 g/mol, is a specialised carbohydrate derivative. This compound finds utility in various chemical research and synthesis applications. Its structure as a protected glucosamine analogue makes it a valuable building block in carbohydrate chemistry and related fields, contributing to advancements in biochemical studies and the development of novel compounds.
- IUPAC
- 2-Propen-1-yl 2-(acetylamino)-2-deoxy-α-D-glucopyranoside
- Synonyms
- 2-Propen-1-yl 2-(acetylamino)-2-deoxy-α-D-glucopyranoside
Chemical Synthesis
Serves as a key intermediate or building block in the synthesis of more complex carbohydrate-based molecules. Its protected nature allows for selective modifications in multi-step organic synthesis.
Carbohydrate Chemistry Research
Utilised in academic and industrial research to study glycosylation reactions, enzyme mechanisms, and the synthesis of glycoconjugates. Its specific structure aids in understanding carbohydrate interactions.
Biochemical Studies
Employed in investigations related to biological processes involving carbohydrates, such as cell recognition and signalling pathways. It can be a tool for probing biological systems.
| Molecular weight | 261.27 |
|---|---|
| Empirical formula | C11H19NO6 |
| Melting point | 167-177 °C |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside used for?
+
Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside is primarily used in chemical synthesis, carbohydrate chemistry research, and biochemical studies as a specialised building block.
What is the CAS number and formula for Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside?
+
The CAS number is 54400-75-8 and the empirical formula is C11H19NO6.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this compound for research and laboratory purposes. The specific grade and purity are available upon request, and we do not represent it as USP, BP, or EP grade unless explicitly stated.
How should Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside be handled and stored?
+
This compound has a WGK Germany rating of 3, indicating it is hazardous to water. Handle with appropriate personal protective equipment in a well-ventilated area and store according to standard laboratory chemical practices, away from incompatible materials.
Is Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside shipped internationally?
+
Yes, Tech Serve Solutions is a global supplier and exporter of fine chemicals, pharmaceutical intermediates, and laboratory reagents, including this compound.
How can I request a sample or quote for Allyl 2-acetamido-2-deoxy-α-D-glucopyranoside?
+
To request a sample or obtain a quote, please contact our sales department through the details provided on the Tech Serve Solutions website.
▶ Related products
1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis
1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more
3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis
3-Methyl-1,5-pentanediol
Chemical Synthesis
3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis