(R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid TCI E0993

Chemical Identity

Other names: (R)-(-)-2-(4-Ethyl-2,3-dioxopiperazine-1-carboxamido)-2-phenylacetic Acid
CAS No.: 63422-71-9
PubChem: CID 2733658·SID 253660152
Formula: C15H17N3O5
Molecular weight: 319.32 g/mol
Purity: >98.0%(HPLC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-2-phenylacetic acid
SMILES: CCN1CCN(C(=O)C1=O)C(=O)NC(C2=CC=CC=C2)C(=O)O
InChIKey: JQEHQELQPPKXRR-LLVKDONJSA-N
MDL: MDL00799536

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This compound, known as (R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic Acid, is a chiral building block widely used in asymmetric synthesis. It plays a crucial role in laboratories where precise control over stereochemistry is required. Its complex structure, combining a piperazine chain with a benzeneacetic acid group, makes it an essential component in the development of bioactive compounds. Due to its chiral nature, it enables the synthesis of enantiomerically pure molecules, which is vital in pharmaceutical research and organic chemistry.

The compound's unique chemical structure allows for highly specific and efficient chemical reactions. Its chiral properties are particularly valuable in the separation of isomers, a process essential for creating compounds with desired biological activities. Additionally, its chemical stability under standard laboratory conditions ensures ease of handling and storage, making it a reliable choice for researchers. The compound's versatility and effectiveness in asymmetric synthesis have made it a preferred material in various scientific applications.

In Indonesian laboratories, this compound is commonly used by researchers in pharmaceutical and organic chemistry fields. It supports the development of new drugs and specialized chemical compounds. Its role in enabling precise stereoselective reactions makes it a key component in advanced research projects. The compound's availability and reliability contribute to its widespread use in academic and industrial research settings across Indonesia.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 4

Related TCI products

Asymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which is critical in drug development and organic chemistry research.
Chiral Building Block Applications: Its complex structure makes it a preferred choice for constructing molecules with specific stereochemistry.
Pharmaceutical Research: The compound's chiral properties are essential for developing bioactive compounds with targeted biological activities.
Organic Chemistry Studies: It supports the synthesis of complex molecules, enabling researchers to explore new chemical reactions and pathways.
Isomer Separation Processes: Its chiral nature allows for the efficient separation of isomers, which is vital in advanced synthetic chemistry techniques.

Brand	TCI
CAS number	63422-71-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, crystalline appearance
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and air. Due to its chiral nature, it is important to handle it with care to avoid contamination or degradation. Standard laboratory safety practices should be followed, including the use of personal protective equipment when handling. The compound is generally stable under normal laboratory conditions, making it suitable for long-term storage and routine use in research settings.

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