(1R,2R)-2-(dimethylamino)cyclohexanol

95%

Reagent Code: #230714
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CAS Number 15910-74-4

science Other reagents with same CAS 15910-74-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.23 g/mol
Formula C₈H₁₇NO
badge Registry Numbers
MDL Number MFCD11520522
inventory_2 Storage & Handling
Storage 2-8℃, inert gas storage

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and central nervous system agents. Its stereochemistry makes it valuable in chiral synthesis where specific enantiomeric forms are required for biological activity. Commonly employed in the development of antitussive drugs and as a building block in the preparation of more complex amine-containing molecules. Also utilized in research settings for asymmetric synthesis and catalysis due to its structural rigidity and functional group compatibility.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,000.00
1g
10-20 days ฿4,980.00
5g
10-20 days ฿17,430.00
(1R,2R)-2-(dimethylamino)cyclohexanol
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and central nervous system agents. Its stereochemistry makes it valuable in chiral synthesis where specific enantiomeric forms are required for biological activity. Commonly employed in the development of antitussive drugs and as a building block in the preparation of more complex amine-containing molecules. Also utilized in research settings for asymmetric synthesis and catalysis du

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of local anesthetics and central nervous system agents. Its stereochemistry makes it valuable in chiral synthesis where specific enantiomeric forms are required for biological activity. Commonly employed in the development of antitussive drugs and as a building block in the preparation of more complex amine-containing molecules. Also utilized in research settings for asymmetric synthesis and catalysis due to its structural rigidity and functional group compatibility.

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