CymitQuimica logo

CAS 1076197-02-8

:

α-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3,4-dimethoxybenzenepropanoic acid

Description:
α-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3,4-dimethoxybenzenepropanoic acid, commonly referred to as Fmoc-amino acid derivatives, is a chemical compound characterized by its complex structure that includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely used in peptide synthesis. This compound features an amino acid backbone with a propanoic acid side chain, along with methoxy groups that enhance its solubility and reactivity. The Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis of peptides. The presence of methoxy groups contributes to the compound's hydrophobic characteristics, influencing its interactions in biological systems. This compound is typically utilized in organic synthesis and biochemistry, particularly in the field of peptide synthesis, where it aids in the formation of peptide bonds while preventing unwanted reactions. Its stability under basic conditions and ease of removal under mild acidic conditions make it a valuable tool in synthetic chemistry.
Formula:C27H27NO6
InChI:InChI=1S/C27H27NO6/c1-32-24-12-11-17(14-25(24)33-2)13-18(26(29)30)15-28-27(31)34-16-23-21-9-5-3-7-19(21)20-8-4-6-10-22(20)23/h3-12,14,18,23H,13,15-16H2,1-2H3,(H,28,31)(H,29,30)
InChI key:InChIKey=ZGOFWUMBCCURJY-UHFFFAOYSA-N
SMILES:C(OC(NCC(CC1=CC(OC)=C(OC)C=C1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • α-[[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3,4-dimethoxybenzenepropanoic acid
  • Benzenepropanoic acid, α-[[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]methyl]-3,4-dimethoxy-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.