cis-4-Aminocyclohexanol

98%

Reagent Code: #137132
label
Alias Related CAS No.: 6850-65-3 (cis-reverse mix); 27489-62-9 (trans); cis-p-aminocyclohexanol
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CAS Number 40525-78-8

science Other reagents with same CAS 40525-78-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.170 g/mol
Formula C₆H₁₃NO
badge Registry Numbers
MDL Number MFCD09997786
thermostat Physical Properties
Boiling Point 201.1±33.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.037 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and muscle relaxants. Its structural configuration allows for selective binding in biological systems, making it valuable in creating chiral drugs. Also employed in the preparation of specialty polymers and ligands for catalysis due to its functional groups and stereochemistry.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE white to yellow solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,180.00
5g
10-20 days ฿5,500.00
25g
10-20 days ฿23,850.00
cis-4-Aminocyclohexanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and muscle relaxants. Its structural configuration allows for selective binding in biological systems, making it valuable in creating chiral drugs. Also employed in the preparation of specialty polymers and ligands for catalysis due to its functional groups and stereochemistry.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and muscle relaxants. Its structural configuration allows for selective binding in biological systems, making it valuable in creating chiral drugs. Also employed in the preparation of specialty polymers and ligands for catalysis due to its functional groups and stereochemistry.

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