(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid

Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid
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CAS No. 737007-45-3
Cat. No. CS-W021155
Purity≥97%
MDL No.None

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid|CS-W021155

Structure of 737007-45-3

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General Information

CAS No. 737007-45-3
Cat. No. CS-W021155
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₅H₂₁N₃O₄
Molecular Weight 427.45
Synonym(s) N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)-L-alanine
SMILES O=C(O)[C@@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CC4=CNC5=NC=CC=C54

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid serves as a versatile chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient N-terminal protection in solid-phase peptide synthesis, while the pyrrolo[2,3-b]pyridine moiety provides a rigid, pharmacophoric core with demonstrated utility in kinase inhibitor scaffolds. The molecule exhibits excellent bench stability, facilitates straightforward purification via flash chromatography, and tolerates a wide range of functional groups under standard coupling conditions.

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 104.31
LogP 4.0973
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-(1H-pyrrolo[2,3-b]pyridin-3-yl)propanoic acid

CAS No. 737007-45-3

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