(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid

Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid
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CAS No. 172169-88-9
Cat. No. CS-0100984
Molecule weight404.25
Purity≥95%
MDL No.MFCD03426235

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid|CS-0100984

Structure of 172169-88-9

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General Information

CAS No. 172169-88-9
Cat. No. CS-0100984
Purity ≥95%
MDL No. MFCD03426235
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₉H₁₈BrNO₄
Molecular Weight 404.25
Synonym(s) Fmoc-(S)-2-amino-4-bromobutyric acid
SMILES O=C(O)[C@@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CCBr

Description

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid features a chiral backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling efficient solid-phase peptide synthesis. The pendant bromo substituent provides a handle for downstream functionalization via transition-metal-catalyzed coupling. This derivative combines stability under standard conditions with orthogonal reactivity, facilitating the incorporation of non-canonical amino acids into biologically active peptides.

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 3.7633
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 6

Other Classifications

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Life Science Amino Acids and their Derivatives Alanine and derivatives

Chemical Biology Peptide Chemistry Amine Protection

Chemical Biology Peptide Chemistry Unnatural Amino Acid Derivatives

Key Words

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-bromobutanoic acid

CAS No. 172169-88-9

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