tert-butyl (R)-(2-hydroxy-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamate

Name: tert-butyl (R)-(2-hydroxy-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamate
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CAS No. 2156591-03-4
Cat. No. CS-1006956
Purity≥97%
MDL No.None

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tert-butyl (R)-(2-hydroxy-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamate|CS-1006956

Structure of 2156591-03-4

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General Information

CAS No. 2156591-03-4
Cat. No. CS-1006956
Purity ≥97%
MDL No. None
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₇H₂₂N₂O₃S
Molecular Weight 334.43
Synonym(s) None
SMILES CC1=C(C2=CC=C([C@@H](NC(OC(C)(C)C)=O)CO)C=C2)SC=N1

Description

This chiral carbamate features a tert-butyl-protected amine linked to a hydroxyethyl group bearing a 4-methylthiazol-5-yl-substituted phenyl moiety. The stereochemistry at the benzylic center enables selective synthetic transformations, while the tert-butyl group provides stability and ease of removal under mild acidic conditions. This compound serves as a key intermediate in the synthesis of bioactive molecules with defined spatial orientation.

Application

tert-Butyl (R)-(2-hydroxy-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamate serves as a stable, bench-ready chiral building block for medicinal chemistry applications. The protected hydroxyl group enables selective transformations, while the pendant thiazole moiety provides a rigid, electron-rich heterocyclic scaffold. It functions effectively in asymmetric synthesis, facilitating stereoselective C–C and C–heteroatom bond formations under standard conditions. The carbamate group offers orthogonal protection and ease of removal, supporting streamlined downstream derivatization.

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 71.45
LogP 3.67662
H_Acceptors 5
H_Donors 2
Rotatable_Bonds 4

Other Classifications

Building Blocks Functional Group Alcohol

Building Blocks Functional Group Amide

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aromatic heterocycle compounds Thiazole compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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tert-butyl (R)-(2-hydroxy-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamate

CAS No. 2156591-03-4

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