(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride

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Reagent Code: #37975
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CAS Number 34582-30-4

science Other reagents with same CAS 34582-30-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.70 g/mol
Formula C₉H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD05662354
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring both tert-butyl and methyl ester groups, makes it a valuable building block for creating enantiomerically pure compounds. It is often employed in asymmetric synthesis to produce amino acid derivatives, which are crucial in the design of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its hydrochloride form enhances solubility, facilitating its use in various organic reactions and purification processes. The compound’s stability and reactivity also make it suitable for research in peptide chemistry and medicinal chemistry, where precise stereochemical control is essential.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,629.00
inventory 250mg
10-20 days ฿360.00
inventory 1g
10-20 days ฿396.00
inventory 10g
10-20 days ฿2,835.00

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(S)-1-tert-Butyl 4-methyl 2-aminosuccinate hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring both tert-butyl and methyl ester groups, makes it a valuable building block for creating enantiomerically pure compounds. It is often employed in asymmetric synthesis to produce amino acid derivatives, which are crucial in the design of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally,

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of chiral molecules. Its structure, featuring both tert-butyl and methyl ester groups, makes it a valuable building block for creating enantiomerically pure compounds. It is often employed in asymmetric synthesis to produce amino acid derivatives, which are crucial in the design of drugs targeting neurological disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its hydrochloride form enhances solubility, facilitating its use in various organic reactions and purification processes. The compound’s stability and reactivity also make it suitable for research in peptide chemistry and medicinal chemistry, where precise stereochemical control is essential.

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