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CAS 288617-77-6

:

(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid

Description:
The chemical substance known as (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-hept-6-enoic acid, with the CAS number 288617-77-6, is a synthetic compound primarily used in peptide synthesis and as a protecting group in organic chemistry. It features a fluorenylmethoxycarbonyl (Fmoc) group, which is commonly employed to protect amino groups during peptide synthesis due to its stability and ease of removal. The compound has a heptenoic acid backbone, indicating the presence of a double bond within a seven-carbon chain, which contributes to its reactivity and potential applications in organic synthesis. The stereochemistry at the 2-position is specified as (2R), indicating that it has a specific spatial arrangement that can influence its biological activity and interactions. Overall, this compound is significant in the field of medicinal chemistry and peptide research, where precise modifications of amino acids are crucial for developing therapeutic agents.
Formula:C23H25NO4
InChI:InChI=1/C23H25NO4/c1-3-4-9-14-23(2,21(25)26)24-22(27)28-15-20-18-12-7-5-10-16(18)17-11-6-8-13-19(17)20/h3,5-8,10-13,20H,1,4,9,14-15H2,2H3,(H,24,27)(H,25,26)/t23-/m1/s1
SMILES:C=CCCC[C@](C)(C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • (R)-N-Fmoc-2-(4-pentenyl)alanine
  • L B656 HHJ H1OVMX1&VQ4U1 &&R Form
  • Fmoc-(R)-2-amino-2-methylhept-6-enoic acid
  • (R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-2-Methyl-Hept-6-Enoic acid
  • (R)-2-{[(9H-fluoren-9-yl)methoxy] carbonylamino}-2-methylhept-6-enoic acid
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