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CAS 211682-15-4

:

(2R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methylpropanoic acid

Description:
The chemical substance known as (2R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methylpropanoic acid, with the CAS number 211682-15-4, is a derivative of amino acids, specifically a protected form of a branched-chain amino acid. It features a fluorenylmethoxycarbonyl (Fmoc) group, which is commonly used in peptide synthesis as a protective group for the amino functionality. This compound exhibits characteristics typical of amino acids, including the presence of both an amino group and a carboxylic acid group, allowing it to participate in peptide bond formation. The Fmoc group provides stability during synthesis and can be removed under basic conditions, facilitating the assembly of peptides. The presence of the methyl group on the second carbon contributes to its branched structure, influencing its steric properties and potentially its biological activity. Overall, this compound is significant in the field of organic chemistry and biochemistry, particularly in the synthesis of peptides and related compounds.
Formula:C19H19NO4
InChI:InChI=1S/C19H19NO4/c1-12(18(21)22)10-20-19(23)24-11-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,12,17H,10-11H2,1H3,(H,20,23)(H,21,22)/t12-/m1/s1
InChI key:InChIKey=BMUDOYSTGJHGNI-GFCCVEGCSA-N
SMILES:C(OC(NC[C@H](C(O)=O)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpropanoicacid
  • Propanoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-, (2R)-
  • (2R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methylpropanoic acid
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