(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid

Name: (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid
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CAS No. 270062-91-4
Cat. No. CS-W011660
Purity≥98%
MDL No.MFCD01861021

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid|CS-W011660

Structure of 270062-91-4

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General Information

CAS No. 270062-91-4
Cat. No. CS-W011660
Purity ≥98%
MDL No. MFCD01861021
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₆H₂₅NO₄
Molecular Weight 415.48
Synonym(s) N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-METHYLPHENYL)ALANINE
SMILES O=C(O)C[C@@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CC4=CC=CC=C4C

Description

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid is a chiral, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group and an ortho-tolyl substituent. This configuration enables efficient incorporation into peptide synthesis workflows, where the Fmoc group facilitates orthogonal deprotection and the sterically hindered side chain enhances sequence fidelity during coupling steps.

Application

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid serves as a valuable chiral building block for the synthesis of bioactive peptides and pharmaceutical intermediates. The Fmoc group enables efficient solid-phase peptide synthesis, while the (S)-configured α-amino acid side chain provides stereochemical control. Its bench-stable nature and compatibility with standard coupling conditions facilitate reliable purification and integration into complex molecular architectures.

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-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 75.63
LogP 4.91952
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 7

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Functional Group Carboxylic Acid

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Life Science Amino Acids and their Derivatives Phenylalanine and derivatives

Chemical Biology Peptide Chemistry Unnatural Amino Acid Derivatives

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(o-tolyl)butanoic acid

CAS No. 270062-91-4

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