CymitQuimica logo

CAS 203854-59-5

:

(2S)-2-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methylbutanoic acid

Description:
The chemical substance known as (2S)-2-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methylbutanoic acid, with the CAS number 203854-59-5, is a derivative of amino acids, specifically a protected form of a leucine analogue. This compound features a fluorenylmethoxycarbonyl (Fmoc) group, which is commonly used in peptide synthesis as a protective group for amino acids. The presence of the Fmoc group allows for selective reactions while preventing unwanted side reactions during the synthesis process. The molecule has a chiral center at the second carbon, indicating that it exists in a specific stereoisomeric form, which is crucial for biological activity. Additionally, the structure includes a carboxylic acid functional group, contributing to its acidity and potential interactions in biological systems. Overall, this compound is significant in the field of organic chemistry and biochemistry, particularly in the synthesis of peptides and other complex molecules. Its unique structural features make it a valuable tool in research and pharmaceutical applications.
Formula:C21H23NO4
InChI:InChI=1S/C21H23NO4/c1-13(2)18(20(23)24)11-22-21(25)26-12-19-16-9-5-3-7-14(16)15-8-4-6-10-17(15)19/h3-10,13,18-19H,11-12H2,1-2H3,(H,22,25)(H,23,24)/t18-/m1/s1
InChI key:InChIKey=WVHQNPPGMKCPTP-GOSISDBHSA-N
SMILES:C(OC(NC[C@H](C(C)C)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (2S)-2-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methylbutanoic acid
  • (S)-2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)-3-methylbutanoic acid
  • Butanoic acid, 2-[[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methyl-, (S)-
  • (s)-2-[(9H-Fluoren-9-ylmethoxycarbonylamino)-methyl]-3-methyl-butyric acid
  • Butanoic acid, 2-[[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3-methyl-, (2S)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.