tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate

Name: tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate
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CAS No. 1298101-47-9
Cat. No. CS-0008344
Purity≥97%
MDL No.MFCD24469814

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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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tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate|CS-0008344

Structure of 1298101-47-9

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General Information

CAS No. 1298101-47-9
Cat. No. CS-0008344
Purity ≥97%
MDL No. MFCD24469814
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₂N₂O₂
Molecular Weight 214.30
Synonym(s) tert-butyl (1S,3R)-3-aMinocyclohexylcarbaMate
SMILES O=C(OC(C)(C)C)N[C@@H](CCC1)C[C@@H]1N

Description

tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate is a chiral, bench-stable building block featuring a protected primary amine on a rigid cyclohexyl scaffold. This configuration enables stereocontrolled synthesis in medicinal chemistry, particularly for constrained peptidomimetics and kinase inhibitors. The tert-butyl carbamate group facilitates selective deprotection under mild acidic conditions, streamlining downstream functionalization.

Application

tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to cyclohexyl-containing scaffolds. The protected amine functionality offers excellent bench stability and compatibility with diverse coupling reactions, while the rigid trans-decalin-like geometry supports stereocontrolled synthesis. Its ease of deprotection and broad functional group tolerance make it ideal for constructing bioactive molecules and heterocyclic frameworks in API 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-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 64.35
LogP 1.781
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Fatty ring compounds Cyclohexane compounds

Key Words

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tert-Butyl N-[(1S,3R)-3-aminocyclohexyl]carbamate

CAS No. 1298101-47-9

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