(2R,3R,4R,5S)-1-Benzyl-2-(hydroxymethyl)piperidine-3,4,5-triol

95%

Reagent Code: #230902
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CAS Number 72458-46-9

science Other reagents with same CAS 72458-46-9

blur_circular Chemical Specifications

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Weight 253.29 g/mol
Formula C₁₃H₁₉NO₄
badge Registry Numbers
MDL Number MFCD30185871
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of glycosidase inhibitors, this compound serves as a key intermediate in developing pharmaceuticals for diabetes treatment. It mimics sugar molecules, interfering with carbohydrate metabolism enzymes. Its structure supports design of drugs that regulate blood glucose by slowing breakdown of complex sugars. Also explored in antiviral research due to its ability to disrupt viral glycoprotein processing. Commonly utilized in medicinal chemistry for designing iminosugars with enhanced selectivity and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,330.00
inventory 250mg
10-20 days ฿26,830.00
inventory 1g
10-20 days ฿53,660.00

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(2R,3R,4R,5S)-1-Benzyl-2-(hydroxymethyl)piperidine-3,4,5-triol
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Used in the synthesis of glycosidase inhibitors, this compound serves as a key intermediate in developing pharmaceuticals for diabetes treatment. It mimics sugar molecules, interfering with carbohydrate metabolism enzymes. Its structure supports design of drugs that regulate blood glucose by slowing breakdown of complex sugars. Also explored in antiviral research due to its ability to disrupt viral glycoprotein processing. Commonly utilized in medicinal chemistry for designing iminosugars with enhanced s

Used in the synthesis of glycosidase inhibitors, this compound serves as a key intermediate in developing pharmaceuticals for diabetes treatment. It mimics sugar molecules, interfering with carbohydrate metabolism enzymes. Its structure supports design of drugs that regulate blood glucose by slowing breakdown of complex sugars. Also explored in antiviral research due to its ability to disrupt viral glycoprotein processing. Commonly utilized in medicinal chemistry for designing iminosugars with enhanced selectivity and bioavailability.

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