CAS 882847-34-9 FMoc-21-aMino-4,7,10,13,16,19-hexaoxaheneicosanoic acid, 98%

NAVIGATION

FMoc-21-aMino-4,7,10,13,16,19-hexaoxaheneicosanoic acid, 98%

PRICE INQUIRY

Catalog Number

ACM882847349-2

CAS Number

882847-34-9

Product Name

FMoc-21-aMino-4,7,10,13,16,19-hexaoxaheneicosanoic acid, 98%

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, 98% serves as a versatile building block for synthetic chemistry, particularly in the creation of cyclic megamolecules and both L- and D-oligopeptides that exhibit circularly polarized luminescence. This compound, characterized as a PEGylated linker with an Fmoc-protected amine and a terminal carboxylic acid, enhances solubility in aqueous environments due to its hydrophilic PEG spacer. Under basic conditions, the Fmoc group can be removed to expose the free amine, allowing for further conjugation reactions. Additionally, the terminal carboxylic acid can react with primary amine groups in the presence of activating agents such as EDC or HATU to form stable amide bonds.

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