(1R,2R)-2-(Methylthio)cyclohexan-1-ol

95%

Reagent Code: #232014
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CAS Number 134108-72-8

science Other reagents with same CAS 134108-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.25 g/mol
Formula C₇H₁₄OS
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive agents. Its stereochemistry makes it valuable for creating enantiomerically pure compounds. The sulfur-containing functional group allows for further chemical modifications, such as oxidation to sulfoxides or sulfones, enabling diverse derivatization pathways in medicinal chemistry. Also employed in asymmetric synthesis and as a ligand precursor in catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,020.00
inventory 250mg
10-20 days ฿19,720.00
inventory 500mg
10-20 days ฿34,130.00
inventory 1g
10-20 days ฿43,980.00
(1R,2R)-2-(Methylthio)cyclohexan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive agents. Its stereochemistry makes it valuable for creating enantiomerically pure compounds. The sulfur-containing functional group allows for further chemical modifications, such as oxidation to sulfoxides or sulfones, enabling diverse derivatization pathways in medicinal chemistry. Also employed in asymmetric synthesis and as a ligand precursor in cata

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of centrally acting muscle relaxants and neuroactive agents. Its stereochemistry makes it valuable for creating enantiomerically pure compounds. The sulfur-containing functional group allows for further chemical modifications, such as oxidation to sulfoxides or sulfones, enabling diverse derivatization pathways in medicinal chemistry. Also employed in asymmetric synthesis and as a ligand precursor in catalysis.

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