(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-chlorophenyl)propanoic acid

Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-chlorophenyl)propanoic acid
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CAS No. 1217716-50-1
Cat. No. CS-0197707
Purity≥97%
MDL No.None

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-chlorophenyl)propanoic acid|CS-0197707

Structure of 1217716-50-1

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General Information

CAS No. 1217716-50-1
Cat. No. CS-0197707
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₅H₂₂ClNO₄
Molecular Weight 435.90
Synonym(s) Fmoc-N-Me-Phe(4-Cl)-OH
SMILES C1(C2=C(C=CC=C2)C3=C1C=CC=C3)COC(N([C@H](C(=O)O)CC4=CC=C(C=C4)Cl)C)=O

Description

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-chlorophenyl)propanoic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amine and a para-chlorophenyl group. This structure enables direct incorporation into peptide synthesis workflows, where the Fmoc moiety facilitates orthogonal protection and the sterically defined chiral center supports high diastereoselective coupling. The compound exhibits excellent stability under standard bench conditions and compatibility with common coupling reagents.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-chlorophenyl)propanoic acid serves as a chiral building block for peptide synthesis, enabling efficient N-terminal protection with orthogonal deprotection under mild conditions. The Fmoc group ensures high stability during storage and standard coupling procedures, while the methylamino functionality supports diverse amide bond formations. Its bench-stable crystalline nature facilitates straightforward purification and handling in synthetic 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-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

TPSA 66.84
LogP 5.2166
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 6

Other Classifications

Building Blocks Functional Group Fmoc

Building Blocks Functional Group Chloride

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

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)(methyl)amino)-3-(4-chlorophenyl)propanoic acid

CAS No. 1217716-50-1

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