CAS 882847-34-9 Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid

NAVIGATION

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid

PRICE INQUIRY

Catalog Number

ACM882847349-3

CAS Number

882847-34-9

Product Name

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid

Structure

Category

Polymers

IUPAC Name

3-[2-[2-[2-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid

Molecular Weight

575.6g/mol

Molecular Formula

C30H41NO10

Canonical SMILES

C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCOCCOCCOCCOCCC(=O)O

InChI

InChI=1S/C30H41NO10/c32-29(33)9-11-35-13-15-37-17-19-39-21-22-40-20-18-38-16-14-36-12-10-31-30(34)41-23-28-26-7-3-1-5-24(26)25-6-2-4-8-27(25)28/h1-8,28H,9-23H2,(H,31,34)(H,32,33)

InChI Key

HEGZERUHBVYZPH-UHFFFAOYSA-N

Application

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid serves as a versatile building block in chemical synthesis, particularly effective in the creation of cyclic megamolecules and both L- and D-oligopeptides exhibiting circularly polarized luminescence. This compound features an Fmoc-protected amine and a terminal carboxylic acid, linked by a hydrophilic PEG chain that enhances solubility in water-based solutions. The Fmoc group can be removed under basic conditions to expose a free amine, enabling further conjugation processes. Additionally, the terminal carboxylic acid is reactive with primary amine groups in the presence of activators such as EDC or HATU, leading to the formation of stable amide bonds, which are crucial in Pegylation reactions.

Complexity

689

Covalently-Bonded Unit Count

Exact Mass

575.273047g/mol

Formal Charge

Heavy Atom Count

Monoisotopic Mass

575.273047g/mol

Rotatable Bond Count

XLogP3

1.7