(S)-methyl 2-(picolinamido)butanoate

95%

Reagent Code: #38608
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CAS Number 1353863-79-2

science Other reagents with same CAS 1353863-79-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.24 g/mol
Formula C₁₁H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD06660120
inventory_2 Storage & Handling
Density 1.152±0.06 g/cm3(Predicted)
Storage 2-8 °C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. It is often employed in the development of pharmaceuticals, where its chiral structure is valuable for creating enantiomerically pure drugs. The compound’s picolinamide group enhances its ability to interact with biological targets, making it useful in the design of enzyme inhibitors or receptor modulators. Additionally, it can be used in research settings to study stereoselective reactions, aiding in the development of new synthetic methodologies. Its ester functionality also allows for further chemical modifications, making it a versatile building block in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,360.00
inventory 100mg
10-20 days ฿5,148.00
inventory 1g
10-20 days ฿18,720.00

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(S)-methyl 2-(picolinamido)butanoate
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This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. It is often employed in the development of pharmaceuticals, where its chiral structure is valuable for creating enantiomerically pure drugs. The compound’s picolinamide group enhances its ability to interact with biological targets, making it useful in the design of enzyme inhibitors or receptor modulators. Additionally, it can be used in research settings to

This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of more complex molecules. It is often employed in the development of pharmaceuticals, where its chiral structure is valuable for creating enantiomerically pure drugs. The compound’s picolinamide group enhances its ability to interact with biological targets, making it useful in the design of enzyme inhibitors or receptor modulators. Additionally, it can be used in research settings to study stereoselective reactions, aiding in the development of new synthetic methodologies. Its ester functionality also allows for further chemical modifications, making it a versatile building block in medicinal chemistry and drug discovery.

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