(S)-4-(1-Aminoethyl)phenol hydrobromide

CAS No. 1001094-89-8
Cat. No. CS-0103184
Molecule weight218.09
Purity≥97%
MDL No.None

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(S)-4-(1-Aminoethyl)phenol hydrobromide|CS-0103184

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General Information

CAS No. 1001094-89-8
Cat. No. CS-0103184
Purity ≥97%
MDL No. None
Storage 4°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₁₂BrNO
Molecular Weight 218.09
Synonym(s) 4-(1-aminoethyl)phenol hydrobromide
SMILES OC1=CC=C([C@@H](N)C)C=C1.[H]Br

Description

(S)-4-(1-Aminoethyl)phenol hydrobromide features a chiral benzylic amine moiety with enhanced solubility and stability in aqueous environments. This bench-stable derivative integrates readily into asymmetric synthesis workflows, offering precise stereocontrol at the α-carbon position. The para-hydroxyl group enables further functionalization via coupling or oxidation reactions.

Application

(S)-4-(1-Aminoethyl)phenol hydrobromide serves as a chiral building block for pharmaceutical intermediates, enabling direct access to aryl-amine-containing scaffolds via standard coupling reactions. The hydrobromide salt enhances solubility and stability in aqueous and polar organic media, facilitating purification and handling. Its functional group tolerance supports downstream transformations including Suzuki-Miyaura coupling and amide formation, making it a practical choice for iterative synthesis in medicinal chemistry 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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

TPSA 46.25
LogP 1.9898
H_Acceptors 2
H_Donors 2
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Phenol

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Key Words

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(S)-4-(1-Aminoethyl)phenol hydrobromide

CAS No. 1001094-89-8

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