L-Aspartic acid 4-tert-butyl ester

98%

  • Product Code: 105283
  Alias:    L-Aspartic acid-4-tert-butyl ester
  CAS:    3057-74-7
Molecular Weight: 189.21 g./mol Molecular Formula: C₈H₁₅NO₄
EC Number: 221-292-8 MDL Number: MFCD00038577
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: L-Aspartic acid 4-tert-butyl ester is widely used in organic synthesis as a building block for peptides and other biologically active compounds. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs targeting neurological disorders and metabolic diseases. The tert-butyl ester group provides protection for the carboxylic acid functionality during synthesis, allowing for selective reactions to occur. This compound is also utilized in the preparation of chiral catalysts and ligands, which are essential in asymmetric synthesis for creating enantiomerically pure substances. Additionally, it finds applications in research and development for studying enzyme mechanisms and protein interactions due to its structural similarity to natural amino acids.
Product Specification:
Test Specification
Purity (HPLC) 98-100
Specific Rotation [A]20/D(C=2 In Meoh) 7-11
Appearance White To Light Yellow Powder
TLC Analysis One Spot
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days Ft11,312.81
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-
25.000 10-20 days Ft49,560.90
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-
L-Aspartic acid 4-tert-butyl ester
L-Aspartic acid 4-tert-butyl ester is widely used in organic synthesis as a building block for peptides and other biologically active compounds. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs targeting neurological disorders and metabolic diseases. The tert-butyl ester group provides protection for the carboxylic acid functionality during synthesis, allowing for selective reactions to occur. This compound is also utilized in the preparation of chiral catalysts and ligands, which are essential in asymmetric synthesis for creating enantiomerically pure substances. Additionally, it finds applications in research and development for studying enzyme mechanisms and protein interactions due to its structural similarity to natural amino acids.
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