Boc-NH-bicyclo[1.1.1]pentane-C-NH2

Name: Boc-NH-bicyclo[1.1.1]pentane-C-NH2
Brand: ChemScene
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CAS No. 1638765-05-5
Cat. No. CS-0047966
Purity≥98%
MDL No.MFCD27987305

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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Boc-NH-bicyclo[1.1.1]pentane-C-NH2|CS-0047966

Structure of 1638765-05-5

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General Information

CAS No. 1638765-05-5
Cat. No. CS-0047966
Purity ≥98%
MDL No. MFCD27987305
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₀N₂O₂
Molecular Weight 212.29
Synonym(s) None
SMILES O=C(OC(C)(C)C)NC12CC(CN)(C1)C2

Description

tert-Butyl N-[3-(aminomethyl)bicyclo[1.1.1]pentan-1-yl]carbamate features a rigid, strain-engineered bicyclo[1.1.1]pentane scaffold that imparts exceptional metabolic stability and conformational restriction. The pendant aminomethyl group enables direct functionalization or coupling in late-stage diversification. This carbamate-protected amine is bench-stable and compatible with standard peptide synthesis protocols.

Application

tert-Butyl N-[3-(aminomethyl)bicyclo[1.1.1]pentan-1-yl]carbamate serves as a stable, bench-friendly amino carbamate building block for medicinal chemistry and synthetic applications. The bicyclo[1.1.1]pentane core imparts exceptional rigidity and metabolic stability, while the tert-butyl carbamate group enables selective protection of primary amines. It facilitates efficient incorporation into complex scaffolds via standard coupling reactions and tolerates diverse functional groups, simplifying purification and enabling direct use in peptide and small-molecule synthesis workflows.

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS05,GHS07
Signal Word : Danger	UN#: 3259
Class : 8	Packing Group : Ⅲ
Hazard Statements : H315-H318-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

TPSA 64.35
LogP 1.3925
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Skeleton Bridge Rings compounds Other bridge ring compounds

Building Blocks Skeleton Fatty ring compounds Cyclobutane compounds

Key Words

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Boc-NH-bicyclo[1.1.1]pentane-C-NH2

CAS No. 1638765-05-5

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