tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate

Name: tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate
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CAS No. 211315-53-6
Cat. No. CS-0142122
Purity≥98%
MDL No.MFCD28334223

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tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate|CS-0142122

Structure of 211315-53-6

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General Information

CAS No. 211315-53-6
Cat. No. CS-0142122
Purity ≥98%
MDL No. MFCD28334223
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₄H₂₀BrNO₂
Molecular Weight 314.22
Synonym(s) tert-butyl (R)-2-(4-bromophenyl)propylcarbamate
SMILES O=C(OC(C)(C)C)NC[C@@H](C1=CC=C(Br)C=C1)C

Description

tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate features a chiral benzylic center with a brominated phenyl group, delivering high stereochemical fidelity. This bench-stable carbamate serves as a protected amine handle in asymmetric synthesis, enabling selective coupling and functionalization under standard conditions.

Application

tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate serves as a stable, bench-ready chiral building block for asymmetric synthesis. The carbamate group enables mild deprotection under acidic conditions, while the pendant 4-bromophenyl moiety supports palladium-catalyzed cross-coupling reactions. Its stereochemical integrity and functional group tolerance make it ideal for constructing biologically relevant scaffolds in medicinal chemistry and process development 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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

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Computational Chemistry Data

TPSA 38.33
LogP 4.0773
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 3

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Functional Group Bromide

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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tert-Butyl (R)-(2-(4-bromophenyl)propyl)carbamate

CAS No. 211315-53-6

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