Oxepanes
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Sigma Aldrich 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]aniline
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Sigma Aldrich epsilon-Caprolactone
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Medchemexpress LLC β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate | 7772-79-4 | ≥97.0% | 389.35 | 5 G
β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars, involving carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
- Used in glycobiology research
- Supports studies of sugar structure, synthesis, biology, and evolution
- Involves carbohydrate chemistry
- Enzymology of glycan formation and degradation
- Protein-glycan recognition
- Role of glycans in biological systems
Medchemexpress LLC β-D-Glucopyranose, 2-(acetylamino)-2-deoxy-, 1,3,4,6-tetraacetate | 7772-79-4 | ≥97.0% | 389.35 | 25 G
β-D-Glucopyranose, 2-(acetylamino)-2-deoxy-, 1,3,4,6-tetraacetate is a biochemical reagent used in glycobiology research. Glycobiology involves the study of the structure, synthesis, biology, and evolution of sugars, including carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is related to basic research, biomedicine, and biotechnology.
- Biochemical reagent for glycobiology research.
- Supports studies in carbohydrate chemistry and glycan enzymology.
- Useful for protein-glycan recognition research.
- Related to basic research, biomedicine, and biotechnology.
- Exhibits antiproliferative activity against DBA/2J mouse friend erythroleukemia cells with an IC50 of 400 μM.
Medchemexpress LLC β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate | 7772-79-4 | ≥97.0% | 389.35 | 100 G
β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate is a biochemical reagent used in glycobiology research. Glycobiology involves the study of the structure, synthesis, biology, and evolution of sugars, including 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.
- Appearance: Solid
- Color: White to off-white
Medchemexpress LLC Beta-D-Glucopyranose, 2-(acetylamino)-2-deoxy, 1,3,4,6-tetraacetate | 7772-79-4 | ≥97.0% | 389.35 | 50 G
Beta-D-Glucopyranose, 2-(acetylamino)-2-deoxy, 1,3,4,6-tetraacetate is a biochemical reagent utilized in glycobiology research, a field dedicated to studying the structure, synthesis, biology, and evolution of sugars. This encompasses carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the intricate role of glycans in biological systems. The compound appears as a white to off-white solid.
- Used in glycobiology research
- Appears as a white to off-white solid
- For research use only
- Has a purity of at least 97.0%
Medchemexpress LLC β-D-Glucopyranose, 2-(acetylamino)-2-deoxy, 1,3,4,6-tetraacetate | 7772-79-4 | ≥97.0% | 389.35 | 10 G
β-D-Glucopyranose,2-(acetylamino)-2-deoxy,1,3,4,6-tetraacetate is a biochemical reagent used in glycobiology research. Glycobiology is 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.
- Class of biochemical reagents.
- Has antiproliferative activity against DBA/2J mouse Friend erythroleukemia cells.
- Available as a white to off-white solid.
Medchemexpress LLC n-Octyl B-D-glucopyr 5g | 29836-26-8 | 292.37 | C14H28O6 | 5 G
n-Octyl β-D-glucopyranoside is a non-ionic detergent used to solubilize and stabilize membrane proteins for biochemical and structural studies. It is commonly applied in membrane protein extraction, solubilization, reconstitution, and crystallization workflows, and can inhibit cavitation-induced cell lysis in vitro.
- Mild, non-denaturing non-ionic detergent for membrane protein work.
- Facilitates solubilization and reconstitution of membrane-bound proteins.
- Suitable for membrane protein crystallization and structural analysis.
- Can inhibit cavitation-induced cell lysis in vitro.
- Powder is stable at refrigerated or frozen conditions for extended storage.
Medchemexpress LLC Epsilon-caprolactone | 502-44-3 | MFCD00003267 | 100.0% | 114.14 g/mol | C6H10O2 | 1 KG
Epsilon-caprolactone is a cyclic ester (lactone) monomer widely used in organic synthesis and polymer chemistry, notably for producing polycaprolactone via ring-opening polymerization. It is a colorless to light yellow liquid (C6H10O2, MW 114.14) with CAS 502-44-3 and is supplied at high purity for research and materials synthesis.
- Used as a monomer for ring-opening polymerization.
- Enables synthesis of biodegradable polycaprolactone.
- High purity suitable for research applications.
- Liquid at room temperature for easy handling.
- Reacts readily in nucleophilic ring-opening reactions.
Medchemexpress LLC n-Octyl B-D-glucopyr 10mM 1mL | 29836-26-8 | 292.37 g/mol | C14H28O6 | 1 ML
n-Octyl β-D-glucopyranoside is a mild, non-ionic detergent used to solubilize membrane-bound proteins, prepare lipid vesicles, and aid membrane protein crystallization. It is supplied in solid and solution formats, including a ready-to-use 10 mM solution in DMSO (1 mL).
- Solubilizes membrane proteins while preserving native structure.
- Non-ionic, non-denaturing detergent suitable for protein reconstitution and crystallization.
- Available as 10 mM solution in DMSO (1 mL) or various solid weights for scale-up.
- Inhibits cavitation-induced cell lysis in vitro, aiding gentle sample handling.
Medchemexpress LLC Epsilon-caprolactone | 502-44-3 | MFCD00003267 | 100.0% | 114.14 g/mol | C6H10O2 | 500 G
ε-Caprolactone is a cyclic ester (lactone) monomer used in ring-opening polymerization to produce polycaprolactone and related polymers. It is used as a building block in organic synthesis and materials research, providing a low-viscosity liquid reagent for polymer chemistry and formulation studies.
- High purity (99.98%).
- Chemical formula C6H10O2, molecular weight 114.14 g/mol.
- Liquid appearance, colorless to light yellow, density ≈1.16 g/cm³.
- Suitable for ring-opening polymerization to produce polycaprolactone.
- Commonly used in polymer synthesis, materials research, and organic synthesis.
Medchemexpress LLC Epsilon-caprolactone | 502-44-3 | MFCD00003267 | 100.0% | 114.14 g/mol | C6H10O2 | 100 G
Epsilon-caprolactone (C6H10O2; MW 114.14 g/mol; CAS 502-44-3) is a six-membered lactone used as a monomer and synthetic building block in organic and polymer chemistry. It is a colorless liquid with high assay suitable for research and synthesis, commonly employed in ring-opening polymerization to produce biodegradable polyesters and copolymers.
- High purity suitable for research-grade synthesis.
- Liquid monomer readily polymerized via ring-opening polymerization.
- Versatile building block for producing biodegradable polyesters and copolymers.
- Compatible with standard organic solvents and common reaction conditions.
- Available with certificate of analysis and safety data sheet for reproducibility and safety.
Medchemexpress LLC Ethyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enyl)acetate | 1166829-70-4 | MFCD18383324 | ≥97.0% | 294.19 g/mol | C16H27BO4 | 250 MG
Bpin-Cyclohexene-C-COOEt is a borylated cyclohexene ethyl ester used as a PROTAC linker and reagent in small-molecule synthesis. It has CAS number 1166829-70-4, molecular formula C16H27BO4, molecular weight 294.19 g/mol, and is supplied with ≥97.0% purity. It is commonly provided in small research pack sizes for laboratory synthesis.
- Borylated cyclohexene ethyl ester useful as a PROTAC linker.
- Documented for use in synthesis of SMARCA2/4 degrader compounds.
- High purity suitable for synthetic chemistry (≥97.0%).
- Available in small research pack sizes, including 250 MG.
- Contains a boronate (Bpin) functional group compatible with cross-coupling reactions.