trans-Methyl 4-formylcyclohexanecarboxylate

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Reagent Code: #209010
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CAS Number 54274-80-5

science Other reagents with same CAS 54274-80-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.21 g/mol
Formula C₉H₁₄O₃
badge Registry Numbers
MDL Number MFCD12965033
thermostat Physical Properties
Boiling Point 236.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and analgesics. Its functional groups allow for selective transformations, making it valuable in constructing complex cyclic structures. Commonly employed in medicinal chemistry for building chiral building blocks and in the preparation of conformationally restricted analogs. Also utilized in research settings for designing novel bioactive molecules and in the optimization of drug candidates requiring specific stereochemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿5,500.00
inventory 5g
10-20 days ฿19,880.00

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trans-Methyl 4-formylcyclohexanecarboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and analgesics. Its functional groups allow for selective transformations, making it valuable in constructing complex cyclic structures. Commonly employed in medicinal chemistry for building chiral building blocks and in the preparation of conformationally restricted analogs. Also utilized in research settings for designing novel bioactive molecules and
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for central nervous system (CNS) drugs and analgesics. Its functional groups allow for selective transformations, making it valuable in constructing complex cyclic structures. Commonly employed in medicinal chemistry for building chiral building blocks and in the preparation of conformationally restricted analogs. Also utilized in research settings for designing novel bioactive molecules and in the optimization of drug candidates requiring specific stereochemistry.
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