CAS 115035-47-7

Boc-Ala-Gly-Gly-OH

Description:

Boc-Ala-Gly-Gly-OH, also known as N-Boc-L-alanylglycylglycine, is a peptide derivative characterized by the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group of L-alanine. This compound consists of three amino acids: alanine (Ala), glycine (Gly), and another glycine (Gly), linked together in a specific sequence. The Boc group serves to protect the amino functionality during peptide synthesis, allowing for selective reactions without interference from the amino group. The presence of glycine, a non-polar amino acid, contributes to the overall hydrophilicity and flexibility of the peptide. This compound is typically utilized in peptide synthesis and research, particularly in the development of peptide-based drugs and in studies involving peptide interactions. Its CAS number, 115035-47-7, allows for precise identification in chemical databases. As with many peptides, its solubility and stability can be influenced by factors such as pH and temperature, making it important to consider these conditions during handling and experimentation.

Formula: C₁₂H₂₁N₃O₆

Synonyms:

• BOC-ALA-GLY-GLY-OH
• N-T-BOC-ALA-GLY-GLY
• {2-[(2S)-2-{[(tert-butoxy)carbonyl]amino}propanamido]acetamido}acetic acid
• (Tert-butoxycarbonyl)-L-alanylglycylglycine
• Glycine, N-[(1,1-dimethylethoxy)carbonyl]-L-alanylglycyl-
• N-[(1,1-Dimethylethoxy)carbonyl]-L-alanylglycylglycine
• Boc-AGG-OH

Boc-Ala-Gly-Gly-OH

CAS: 115035-47-7

Bachem ID: 4009580.

Formula: C₁₂H₂₁N₃O₆

Purity: >98%

Color and Shape: White Powder

Molecular weight: 303.32

Ref: 01-4009580

{2-[(2S)-2-{[(tert-butoxy)carbonyl]amino}propanamido]acetamido}acetic acid

CAS: 115035-47-7

Formula: C₁₂H₂₁N₃O₆

Color and Shape: Solid

Molecular weight: 303.3116

Ref: IN-DA000FRH

Boc-Ala-Gly-Gly-OH

CAS: 115035-47-7

Boc-Ala-Gly-Gly-OH is a reactive compound that can be used to synthesize antibiotics. It can be used for the production of diazide, which is an antibiotic that inhibits bacterial growth by binding to DNA and preventing its replication. Boc-Ala-Gly-Gly-OH also has been used for the preparation of urethanes, which are used as coatings for medical devices or catheters. This compound is chiral and has been shown to have stereogenic properties in catalytic asymmetric epoxidation reactions.

Formula: C₁₂H₂₁N₃O₆

Purity: Min. 95%

Molecular weight: 303.31 g/mol

Ref: 3D-FB111200