4-(Fmoc-amino)-1-methyl-1H-pyrrole-2-carboxylic Acid TCI F1314

Chemical Identity

Other names: Fmoc-Py-OH · 4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-1-methyl-1H-pyrrole-2-carboxylic Acid · 4-(Fmoc-amino)-1-methylpyrrole-2-carboxylic Acid · Fmoc-Py-OH
CAS No.: 195387-29-2
PubChem: CID 2756159
Formula: C21H18N2O4
Molecular weight: 362.39 g/mol
Purity: >97.0%(HPLC)(T)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-(9H-fluoren-9-ylmethoxycarbonylamino)-1-methylpyrrole-2-carboxylic acid
SMILES: CN1C=C(C=C1C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
InChIKey: GHRPKWXGCOWBLD-UHFFFAOYSA-N
MDL: MDL02094546

Rp 1.856.400,00

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4-(Fmoc-amino)-1-methyl-1H-pyrrole-2-carboxylic Acid is a chemical compound widely used in the synthesis of complex molecules, particularly in organic and biochemical research. This compound serves as a fundamental building block in the development of biological molecules such as peptides and proteins. Its ability to form bonds with other functional groups makes it a versatile tool for molecular construction. In the laboratory, it is essential for creating intricate molecular structures that are critical in various scientific investigations.

The compound is valued for its chemical stability and reactivity, which enable a wide range of chemical reactions, including substitution, bond formation, and functional group modification. Its complex molecular structure also makes it ideal for synthesizing compounds with biological activity. These properties make it a preferred choice for researchers requiring precision and control in their experiments. Its reliability and consistency ensure reproducibility in laboratory settings, making it a trusted component in chemical synthesis.

In Indonesian laboratories, this compound is commonly used in chemical, pharmaceutical, and biotechnology research. Local scientists frequently employ it for drug development, biological compound modification, and molecular interaction studies. Its availability in the local market supports ongoing research efforts, contributing to advancements in science and innovation.

TCI brochures (PDF)

Raw Materials for the Synthesis of Pyrrole–imidazole Polyamide to Recognize DNA Sequences 2025-06-10 · p. 1

Related TCI products

Peptide Synthesis: This compound is ideal for peptide synthesis due to its ability to form stable amide bonds with amino acids, enabling the creation of complex peptide sequences.
Protein Modification: It is used in protein modification to introduce specific functional groups, enhancing the compound's reactivity and utility in biochemical studies.
Drug Development: Researchers use it in drug development to design molecules with targeted biological activities, supporting the creation of new therapeutic agents.
Molecular Interaction Studies: Its complex structure allows for the study of molecular interactions, aiding in understanding biological processes and molecular behavior.
Organic Chemistry Research: It serves as a key building block in organic chemistry, facilitating the synthesis of a wide range of complex organic compounds.

Brand	TCI
CAS number	195387-29-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (as per standard chemical product form)
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. Proper labeling of containers is essential for safe handling and identification. In laboratory settings, personal protective equipment such as gloves and safety goggles should be worn when handling the compound to ensure safety. It should be kept in a well-ventilated area to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications.

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