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CAS 332121-92-3

:

2-(Fmoc-amino)-4-chlorobenzoic acid

Description:
2-(Fmoc-amino)-4-chlorobenzoic acid is a chemical compound characterized by its structure, which includes a benzoic acid moiety substituted with a chlorinated aromatic ring and a fluorenylmethyloxycarbonyl (Fmoc) protecting group on the amino group. This compound is often utilized in peptide synthesis as a building block due to the stability of the Fmoc group, which can be selectively removed under basic conditions. The presence of the chlorine atom at the para position enhances its reactivity and can influence the compound's solubility and interaction with other molecules. It typically appears as a solid and is soluble in organic solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF). The compound's molecular structure allows for various functionalization and modifications, making it valuable in medicinal chemistry and bioconjugation applications. Safety data should be consulted for handling, as with many organic compounds, and proper laboratory protocols should be followed to ensure safe usage.
Formula:C22H16ClNO4
InChI:InChI=1/C22H16ClNO4/c23-13-9-10-18(21(25)26)20(11-13)24-22(27)28-12-19-16-7-3-1-5-14(16)15-6-2-4-8-17(15)19/h1-11,19H,12H2,(H,24,27)(H,25,26)
InChI key:InChIKey=BIPQSYSWHUYDEA-UHFFFAOYSA-N
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=Nc1cc(ccc1C(=O)O)Cl)O
Synonyms:
  • 2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-chlorobenzoic acid
  • 4-chloro-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}benzoic acid
  • Benzoic acid, 4-chloro-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-
  • N-(9-Fluorenylmethoxycarbonyl)-4-chloroanthranilic acid~N-Fmoc-4-chloroanthranilic acid
  • N-Fmoc-4-chloroanthranilic acid
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