rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate

Name: rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate
Brand: ChemScene
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CAS No. 1425254-01-8
Cat. No. CS-0058294
Purity≥98%
MDL No.None

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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+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
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rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate|CS-0058294

Structure of 1425254-01-8

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General Information

CAS No. 1425254-01-8
Cat. No. CS-0058294
Purity ≥98%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₁H₂₁NO₃
Molecular Weight 215.29
Synonym(s) tert-butyl N-[cis-3-hydroxycyclohexyl]carbamate
SMILES O=C(OC(C)(C)C)N[C@H]1C[C@@H](O)CCC1

Description

rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate is a stereochemically defined cyclohexanol derivative featuring a protected amine and a hydroxyl group in a trans-oriented configuration. This chiral scaffold enables selective functionalization in asymmetric synthesis, particularly in the construction of complex natural products and pharmaceutical intermediates. The tert-butyl carbamate group provides stability and facilitates orthogonal deprotection under mild conditions.

Application

rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate serves as a stereochemically defined chiral building block for cyclohexane-based scaffolds. The (1R,3S) configuration provides predictable conformational control in cyclic systems, while the protected amine and hydroxyl groups enable orthogonal functionalization. It facilitates efficient access to complex polycyclic structures through selective transformations, with bench stability and straightforward purification supporting its utility in medicinal chemistry synthesis.

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 : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

Quality Control

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Computational Chemistry Data

TPSA 58.56
LogP 1.8146
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Functional Group Alcohol

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Fatty ring compounds Cyclohexane compounds

Key Words

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rel-tert-Butyl ((1R,3S)-3-hydroxycyclohexyl)carbamate

CAS No. 1425254-01-8

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