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TCI

CAS 144120-54-7

1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate TCI A2909

1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate TCI A2909

Chemical Identity

CAS No.
144120-54-7
PubChem
CID 7020606·SID 253661157
Formula
C23H23NO6
Molecular weight
409.4 g/mol
Purity
>96.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-5-oxo-5-prop-2-enoxypentanoic acid
SMILES
C=CCOC(=O)[C@H](CCC(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey
ORKKMGRINLTBPC-FQEVSTJZSA-N
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1-Allyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-glutamate is a complex chemical compound widely used in biochemical and peptide synthesis applications. This compound serves as a key building block in the development of bioactive molecules and is essential for researchers working on peptide modification and functional molecule design. Its unique molecular structure, featuring a glutamate residue linked to a modified carbonyl group, allows for versatile chemical interactions, making it a valuable tool in synthetic chemistry. In laboratory settings, this compound is frequently employed to create compounds with specific biological activities, supporting advancements in pharmaceutical and biotechnological research.

The compound’s molecular complexity and functional groups make it a preferred choice for high-precision chemical synthesis. Its ability to participate in various chemical reactions and interact with different reagents and catalysts enhances its utility in laboratory experiments. The presence of the allyl group and the fluorenyl methoxy carbonyl moiety provides structural versatility, enabling researchers to tailor its properties for specific applications. These characteristics make it a reliable and effective reagent for advanced chemical and biochemical studies.

In Indonesian laboratories, this compound is commonly used in chemical and molecular biology research. It is a key component in studies related to bioactive compound development and peptide synthesis. Its availability in the local market supports research institutions and universities in conducting experiments that require high-quality chemical reagents. The compound is widely utilized in academic and industrial research settings, contributing to the advancement of scientific knowledge in the region.

TCI brochures (PDF)

  • Peptide Synthesis: This compound is ideal for constructing complex peptide sequences due to its functional groups that facilitate coupling reactions.
  • Bioactive Compound Development: Its molecular structure allows for the creation of molecules with specific biological activities, supporting drug discovery efforts.
  • Molecular Biology Research: It is used in studies involving protein modification and functional analysis, aiding in understanding molecular interactions.
  • Chemical Modification Studies: The compound’s reactive groups enable researchers to explore new synthetic pathways and chemical transformations.
  • Academic Research: It is a valuable tool for students and researchers in universities and research institutes working on advanced chemical and biochemical projects.

Brand TCI
CAS number 144120-54-7
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid powder
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 integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its chemical complexity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. The compound is not inherently hazardous under normal storage conditions, but standard laboratory safety protocols should be followed when handling and using it. Proper labeling and storage practices will help maintain the compound’s effectiveness and ensure safe usage in research settings.

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