(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid

Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid
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CAS No. 206060-54-0
Cat. No. CS-0101061
Purity≥97%
MDL No.MFCD01632251

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid|CS-0101061

Structure of 206060-54-0

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General Information

CAS No. 206060-54-0
Cat. No. CS-0101061
Purity ≥97%
MDL No. MFCD01632251
Storage RT, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₆H₂₅NO₅
Molecular Weight 431.48
Synonym(s) Fmoc-L-(2,6-di-Me)Tyr-OH
SMILES OC(C=C1C)=CC(C)=C1C[C@@H](C(O)=O)NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O

Description

This fluorenylmethoxycarbonyl-protected chiral amino acid derivative features a sterically hindered para-hydroxyaryl side chain and a bench-stable carbamate group, enabling direct incorporation into peptide synthesis workflows without racemization.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid serves as a valuable chiral building block in peptide synthesis and medicinal chemistry. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions. The pendant phenolic hydroxyl and methylated aromatic ring provide structural rigidity and enhanced solubility, facilitating purification and downstream functionalization in solid-phase and solution-phase workflows.

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501

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Computational Chemistry Data

TPSA 95.86
LogP 4.54344
H_Acceptors 4
H_Donors 3
Rotatable_Bonds 6

Other Classifications

Building Blocks Functional Group Fmoc

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Chemical Biology Peptide Chemistry Amine Protection

Chemical Biology Peptide Chemistry Unnatural Amino Acid Derivatives

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid

CAS No. 206060-54-0

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