(3R,4R)-3-Amino-4-hydroxypentanoic acid hydrochloride

≥95%

Reagent Code: #36747
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CAS Number 336182-14-0

science Other reagents with same CAS 336182-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.61 g/mol
Formula C₅H₁₂ClNO₃
badge Registry Numbers
MDL Number MFCD01862874
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. It serves as a key chiral building block in the production of molecules with specific stereochemistry, which is crucial for their biological activity. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding due to its structural similarity to naturally occurring amino acids. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and formulations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,503.00
inventory 250mg
10-20 days ฿4,176.00
inventory 5g
10-20 days ฿36,504.00

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(3R,4R)-3-Amino-4-hydroxypentanoic acid hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. It serves as a key chiral building block in the production of molecules with specific stereochemistry, which is crucial for their biological activity. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding due to its structural similarity to naturally occurring amino acids. Its hydrochloride form enhances solubilit

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. It serves as a key chiral building block in the production of molecules with specific stereochemistry, which is crucial for their biological activity. Additionally, it is employed in research settings for studying enzyme inhibition and receptor binding due to its structural similarity to naturally occurring amino acids. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and formulations.

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