(R)-3-Amino-4-(tert-butoxy)butanoic acid

≥95%

Reagent Code: #37621
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CAS Number 1956437-97-0

science Other reagents with same CAS 1956437-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.23 g/mol
Formula C₈H₁₇NO₃
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MDL Number MFCD30180243
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

(R)-3-Amino-4-(tert-butoxy)butanoic acid is primarily utilized in the field of organic synthesis as a chiral building block. Its structure, featuring both an amino group and a tert-butoxy group, makes it a valuable intermediate in the production of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it is used in peptide synthesis and as a precursor for the preparation of complex molecules in medicinal chemistry. The tert-butoxy group provides steric protection, which can be advantageous in selective reactions, while the amino group allows for further functionalization, making it a versatile reagent in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,132.00
inventory 250mg
10-20 days ฿6,264.00

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(R)-3-Amino-4-(tert-butoxy)butanoic acid
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(R)-3-Amino-4-(tert-butoxy)butanoic acid is primarily utilized in the field of organic synthesis as a chiral building block. Its structure, featuring both an amino group and a tert-butoxy group, makes it a valuable intermediate in the production of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it is used

(R)-3-Amino-4-(tert-butoxy)butanoic acid is primarily utilized in the field of organic synthesis as a chiral building block. Its structure, featuring both an amino group and a tert-butoxy group, makes it a valuable intermediate in the production of pharmaceuticals, particularly in the synthesis of enantiomerically pure compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Additionally, it is used in peptide synthesis and as a precursor for the preparation of complex molecules in medicinal chemistry. The tert-butoxy group provides steric protection, which can be advantageous in selective reactions, while the amino group allows for further functionalization, making it a versatile reagent in drug discovery and development processes.

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