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[2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid, 98.5%|190014|166108-71-0

[2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid, 98.5%

Cat. No JK190014_1_G
J&K Chemical

Product Information

Product Name
2-2-(Fmoc-amino)ethoxyethoxyacetic acid, 98.5%
Brand Name
J&K
Product Number
190014
CAS
166108-71-0
Molecular Formula
C21H23NO6
Molecular Weight
385.41
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
Fmoc-AEEA
PubChem CID
2756092
IUPAC Name
2-2-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxyethoxyacetic acid
InChI Key
XQPYRJIMPDBGRW-UHFFFAOYSA-N
SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCC(=O)O

Properties

Melting Point
90-92

Safety Information

Storage Condition
Room temperature

References Data Source From Pubchem

Macrocyclizing-thioesterases in bacterial non-ribosomal peptide biosynthesis
Publication Name: Journal of Natural Medicines
Publication Date: 2024-08-30
DOI: 10.1007/s11418-024-01841-y

A novel peptide-based electrochemical biosensor for the determination of a metastasis-linked protease in pancreatic cancer cells
Publication Name: Analytical and Bioanalytical Chemistry
Publication Date: 2020-01-27
DOI: 10.1007/s00216-020-02418-w

Synthesis and characterization of NH2-(AEEA)n-amphotericin B derivatives
Publication Name: The Journal of Antibiotics
Publication Date: 2019-01-11
DOI: 10.1038/s41429-018-0138-8

Plant cysteine oxidases are dioxygenases that directly enable arginyl transferase-catalysed arginylation of N-end rule targets
Publication Name: Nature Communications
Publication Date: 2017-03-23
DOI: 10.1038/ncomms14690

Differential Carbohydrate Recognition by Campylobacter jejuni Strain 11168: Influences of Temperature and Growth Conditions
Publication Name: PLoS ONE
Publication Date: 2009-03-17
DOI: 10.1371/journal.pone.0004927

[2-[2-(Fmoc-amino)ethoxy]ethoxy]acetic acid, 98.5%

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