(2S,3R,4S,5S,6R)-2-(4-Chloro-3-(4-Ethoxybenzyl)Phenyl)-6-(Hydroxymethyl)-2-Methoxytetrahydro-2H-Pyran-3,4,5-Triol(CAS 714269-57-5)
| Purity | Grade | Package | Stock | Price | Quantity |
| 99% | RG | 250MG | In Stock | 1 USD
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| 99% | RG | 1G | In Stock | 3 USD
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| 99% | RG | 5G | In Stock | 11 USD
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| 99% | RG | 25G | In Stock | 17 USD
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| 99% | RG | 100G | In Stock | 126 USD
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| 99% | RG | 500G | In Stock | 630 USD
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Your region is eligible for ordering. Available NMR Spectrum
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Applications of 714269-57-5
| Industry | Application | Process |
|---|---|---|
| Pharmaceutical Industry | Key Intermediate for SGLT2 Inhibitors: A core intermediate in the synthesis of sodium-glucose co-transporter 2 (SGLT2) inhibitors (e.g., empagliflozin), used to construct the glycosylated structure of the drug molecule. | Pharmaceutical Synthesis: Typically employed as a glycosyl donor in glycosylation reactions with the corresponding aglycone under acidic or Lewis acid catalysis to form C-glycosidic bonds, followed by deprotection to yield the active pharmaceutical ingredient (API). |
| Pharmaceutical Industry | Candidate Drug Development: Used in screening and optimization of novel SGLT2 inhibitors or other antidiabetic candidate drugs. | Organic Synthesis and Structural Modification: Leveraging its hydroxyl groups and reactive hydrogen atoms to conduct esterification, etherification, or substitution reactions, generating derivative series for biological activity evaluation. |
| Scientific Research | Mechanistic Studies of Chemical Reactions: Employed to investigate stereochemical control in glycosylation reactions and synthetic methodologies for C-glycosides. | Methodology Development in Organic Synthesis: Serves as a model substrate to evaluate the impact of novel catalysts or reaction conditions on stereoselectivity (α/β ratio) and yield optimization in glycosylation reactions. |
| Chemical Synthesis | Fine Chemical Synthesis: Used to synthesize structurally complex glycosylated fine chemicals or chiral molecules with specific optical activity. | Chiral Synthesis and Separation Techniques: Exploits its defined stereocenter to prepare optically pure compounds via resolution or asymmetric synthesis. |
Physical and chemical properties of 714269-57-5
Acidity coefficient |
12.59±0.70(Predicted) |
|---|---|
Boiling Point |
609.6±55.0 °C at 760 mmHg |
Density |
1.4±0.1 g/cm3 |
Exact Mass |
438.144531 |
Flash Point |
322.5±31.5 °C |
Index of Refraction |
1.628 |
LogP |
5.58 |
Melting Point |
>80°C (dec.) |
Molecular Formula |
C22H27ClO7 |
Molecular Weight |
438.899 |
PSA |
108.61000 |
Solubility |
Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly), Water (Slightly) |
Stability |
Hygroscopic |
Storage condition |
2-8°C |
Vapour Pressure |
0.0±1.8 mmHg at 25°C |
Spectrums of 714269-57-5
1.The NMR spectrum displayed on the page is a pre-sale reference spectrum and may differ from that of the actual received batch.
2.The accompanying documentation will include the NMR spectrum and purity analysis data for the shipped batch.
Retrosynthesis analysis of 714269-57-5
Cas:32469-28-6
Cas:461432-23-5
Q&A for CAS 714269-57-5
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Yes. Batch COA available matches the actual shipment. COAs shown online are for reference or from previous batches.
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Download SDS of 714269-57-5
Pictograms |
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|---|---|
Signal Word |
Warning |
Hazard Statements |
H302 Harmful if swallowed H315 Causes skin irritation H317 May cause an allergic skin reaction H319 Causes serious eye irritation H373 May causes damage to organs through prolonged or repeated exposure |
Safety Data Sheet |
Download COA of 714269-57-5
Operate under the ISO 9001 system
