tert-Butyl (1-bromopropan-2-yl)carbamate

Name: tert-Butyl (1-bromopropan-2-yl)carbamate
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CAS No. 1391026-59-7
Cat. No. CS-0139502
Purity≥95%
MDL No.MFCD24167884

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tert-Butyl (1-bromopropan-2-yl)carbamate|CS-0139502

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General Information

CAS No. 1391026-59-7
Cat. No. CS-0139502
Purity ≥95%
MDL No. MFCD24167884
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₈H₁₆BrNO₂
Molecular Weight None
Synonym(s) tert-butyl N-(1-bromopropan-2-yl)carbamate
SMILES O=C(OC(C)(C)C)NC(C)CBr

Description

tert-Butyl (1-bromopropan-2-yl)carbamate features a brominated chiral center flanked by a stable tert-butyl carbamate group, enabling direct functionalization in late-stage synthesis. This bench-stable reagent integrates seamlessly into iterative coupling workflows, offering reliable access to complex amine derivatives under standard conditions.

Application

tert-Butyl (1-bromopropan-2-yl)carbamate serves as a stable, bench-ready carbamate protecting group for primary amines, enabling selective N-alkylation and subsequent deprotection under mild acidic conditions. Its bromo substituent provides a versatile handle for further functionalization via palladium-catalyzed cross-coupling reactions. The compound exhibits excellent functional group tolerance and facilitates efficient synthesis of complex amine-containing intermediates in medicinal chemistry and process development workflows.

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P301+P310-P330-P501

Quality Control

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Computational Chemistry Data

TPSA 38.33
LogP 2.2945
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Boc

Building Blocks Functional Group Amine

Building Blocks Functional Group Bromide

Key Words

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tert-Butyl (1-bromopropan-2-yl)carbamate

CAS No. 1391026-59-7

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