(1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane

95%

Reagent Code: #70811
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Alias Eucalyptol
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CAS Number 5718-75-2

science Other reagents with same CAS 5718-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.31 g/mol
Formula C₁₀H₁₈S
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of more complex molecules. Its unique bicyclic structure and stereochemistry make it valuable for constructing optically active compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it can serve as a ligand or catalyst in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Its sulfur-containing moiety also makes it relevant in the development of organosulfur compounds, which have applications in materials science and medicinal chemistry.

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Test Parameter Specification
Appearance Colorless to Almost colorless clear liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,490.00
inventory 5g
10-20 days ฿17,190.00

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(1R,4R,5R)-4,7,7-Trimethyl-6-thiabicyclo[3.2.1]octane
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of more complex molecules. Its unique bicyclic structure and stereochemistry make it valuable for constructing optically active compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it can serve as a ligand or catalyst in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Its sulfur-containing moiety als

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of more complex molecules. Its unique bicyclic structure and stereochemistry make it valuable for constructing optically active compounds, which are essential in pharmaceuticals and agrochemicals. Additionally, it can serve as a ligand or catalyst in asymmetric synthesis, enabling the creation of enantiomerically pure substances. Its sulfur-containing moiety also makes it relevant in the development of organosulfur compounds, which have applications in materials science and medicinal chemistry.

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