(R)-Methyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride

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Reagent Code: #55155
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CAS Number 2049127-84-4

science Other reagents with same CAS 2049127-84-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.77 g/mol
Formula C₁₁H₁₆ClNO₄S
badge Registry Numbers
MDL Number MFCD30570303
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular conditions. The presence of both amino and ester functional groups allows for further chemical modifications, enabling the development of compounds with specific biological activities. Additionally, it is employed in research settings to study the structure-activity relationships of molecules, aiding in the design of more effective and selective therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,105.00
inventory 1g
10-20 days ฿6,210.00

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(R)-Methyl 2-amino-3-(3-(methylsulfonyl)phenyl)propanoate hydrochloride
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular conditions. The presence of both amino and ester functional groups allows for further chemical modifications, enabling the development of compounds with specific biological activities. Additionally, it i

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting neurological and cardiovascular conditions. The presence of both amino and ester functional groups allows for further chemical modifications, enabling the development of compounds with specific biological activities. Additionally, it is employed in research settings to study the structure-activity relationships of molecules, aiding in the design of more effective and selective therapeutic agents.

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