(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide

95%

Reagent Code: #230944
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CAS Number 1448682-03-8

science Other reagents with same CAS 1448682-03-8

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scatter_plot Molecular Information
Weight 227.2816 g/mol
Formula C₁₀H₁₃NO₃S
badge Registry Numbers
MDL Number MFCD28952874
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or condensation, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to introduce chirality and sulfonamide groups, which can enhance binding affinity and metabolic stability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,820.00
inventory 250mg
10-20 days ฿32,000.00

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(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or condensation, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to introduce chirality and sulfonamide groups, which can enhance binding affinity and metabolic stabil

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enantiomerically pure drugs. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or condensation, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its ability to introduce chirality and sulfonamide groups, which can enhance binding affinity and metabolic stability in drug candidates.

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