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AI08719

1115-69-1 | N-Acetyl-DL-alanine

Packsize Purity Availability Price Discounted Price    Quantity
10g 98% in stock $9.00 $6.00 -   +
25g 98% in stock $19.00 $14.00 -   +
100g 98% in stock $69.00 $49.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI08719
Chemical Name: N-Acetyl-DL-alanine
CAS Number: 1115-69-1
Molecular Formula: C5H9NO3
Molecular Weight: 131.1299
MDL Number: MFCD00037238
SMILES: CC(=O)NC(C(=O)O)C

 

Computed Properties
Complexity: 132  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
XLogP3: -0.9  

 

 

Upstream Synthesis Route
  • N-Acetyl-DL-alanine, also known as N-Acetyldlalanine, is a versatile compound commonly used in chemical synthesis. This amino acid derivative plays a crucial role in various chemical reactions and processes due to its unique properties and reactivity.In chemical synthesis, N-Acetyl-DL-alanine is often utilized as a building block or starting material in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its functional groups allow it to participate in a wide range of reactions, such as acylation, amidation, and other transformations that are key steps in organic synthesis.One of the primary applications of N-Acetyl-DL-alanine is in the preparation of peptide derivatives and related compounds. By incorporating N-Acetyl-DL-alanine into the peptide backbone, chemists can introduce specific functionalities and improve the properties of the resulting molecules. This is particularly valuable in drug discovery and development, where the precise control over molecular structure and properties is crucial for optimizing drug efficacy and safety.Furthermore, N-Acetyl-DL-alanine can also serve as a protecting group for amino acids during peptide synthesis. By temporarily masking the reactive amine groups, N-Acetyl-DL-alanine helps to selectively modify specific amino acids without interfering with the overall peptide assembly process. This strategy allows for the efficient and controlled construction of complex peptide sequences with high purity and yield.Overall, the versatile nature of N-Acetyl-DL-alanine makes it a valuable tool in chemical synthesis, enabling chemists to access a wide range of structurally diverse compounds with tailored properties and functions. Its applications extend beyond peptide chemistry to encompass various areas of organic and medicinal chemistry, highlighting its importance in advancing research and innovation in the field of chemical science.
Literature
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