tert-Butyl oct-7-yn-1-ylcarbamate

CAS No. 1451262-84-2
Cat. No. CS-0614536
Purity≥97%
MDL No.MFCD31729564

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tert-Butyl oct-7-yn-1-ylcarbamate|CS-0614536

Structure of 1451262-84-2

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Description

tert-Butyl oct-7-yn-1-ylcarbamate features a terminal alkyne handle flanked by a sterically hindered tert-butyl carbamate group, enabling robust protection and selective coupling in multistep synthesis. This stable, bench-ready reagent facilitates efficient CuAAC reactions and integrates seamlessly into complex molecular architectures requiring orthogonal functionalization.

Application

tert-Butyl oct-7-yn-1-ylcarbamate serves as a robust, bench-stable building block for the synthesis of alkyne-functionalized intermediates. Its terminal alkyne moiety enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), while the tert-butoxycarbonyl (Boc) group provides orthogonal protection for primary amines. The molecule exhibits excellent functional group tolerance and facilitates straightforward purification, making it well-suited for iterative peptide and heterocycle assembly in medicinal chemistry workflows.

General Information

CAS No. 1451262-84-2
Cat. No. CS-0614536
Purity ≥97%
MDL No. MFCD31729564
Storage 4°C, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₃H₂₃NO₂
Molecular Weight 225.33
Synonym(s) N-Boc-oct-7-yn-1-amine
SMILES O=C(OC(C)(C)C)NCCCCCCC#C

Computational Chemistry Data

TPSA 38.33
LogP 3.0948
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 6

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-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Other Classifications

Building Blocks Functional Group Boc

Building Blocks Functional Group Alkyne

Building Blocks Skeleton Fatty chain compounds

Life Science Click Chemistry Reagents Alkyne

Life Science PROTAC PROTAC Linker

Chemical Biology Pharmaceutical Development and Drug Discovery Research Conjugation Chemistry/Click Chemistry Terminal Alkynes

Chemical Biology Pharmaceutical Development and Drug Discovery Research Reagents Proteolysis Targeting Chimera Research Reagents

Chemical Biology Conjugation Chemistry/Click Chemistry Terminal Alkynes

Biochemistry Pharmaceutical Development and Drug Discovery Research Proteolysis Targeting Chimera Research Reagents

Key Words

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tert-Butyl oct-7-yn-1-ylcarbamate

CAS No. 1451262-84-2

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