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CAS 176442-21-0

:

3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-hydroxybenzoic acid

Description:
3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-5-hydroxybenzoic acid, commonly referred to as Fmoc-5-hydroxy-3-amino benzoic acid, is a chemical compound characterized by its structure, which includes a benzoic acid moiety substituted with a hydroxyl group and an amino group protected by a fluorenylmethoxycarbonyl (Fmoc) group. This compound is typically used in peptide synthesis as a building block due to the stability of the Fmoc protecting group under basic conditions, allowing for selective deprotection during the synthesis process. The presence of the hydroxyl group enhances its solubility in polar solvents, making it suitable for various biochemical applications. Additionally, the compound exhibits potential for further functionalization, which can be advantageous in drug development and material science. Its CAS number, 176442-21-0, is a unique identifier that facilitates its identification in chemical databases and literature. Overall, this compound is significant in organic synthesis and medicinal chemistry, particularly in the context of peptide and protein engineering.
Formula:C22H17NO5
InChI:InChI=1/C22H17NO5/c24-15-10-13(21(25)26)9-14(11-15)23-22(27)28-12-20-18-7-3-1-5-16(18)17-6-2-4-8-19(17)20/h1-11,20,24H,12H2,(H,23,27)(H,25,26)
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=Nc1cc(cc(c1)O)C(=O)O)O
Synonyms:
  • 3-Amino-5-hydroxybenzoic acid, N-FMOC protected
  • 3-Amino-5-hydroxybenzoic acid, N-FMOC protected 97%
  • N-Fmoc-3-Amino-5-Hydroxybenzoic Acid
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