Methyl 1-aminocyclohexanecarboxylate hydrochloride

≥97%

Reagent Code: #39922
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CAS Number 37993-32-1

science Other reagents with same CAS 37993-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.67 g/mol
Formula C₈H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD09264353
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting the central nervous system, where its structure can be modified to create compounds with specific therapeutic effects. Additionally, it is employed in research settings for the study of chemical reactions involving cyclohexane derivatives, aiding in the exploration of new synthetic pathways and the optimization of reaction conditions. Its hydrochloride form enhances stability and solubility, making it easier to handle and incorporate into various chemical processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿702.00
inventory 1g
10-20 days ฿1,674.00
inventory 5g
10-20 days ฿5,166.00
inventory 10g
10-20 days ฿5,796.00
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Methyl 1-aminocyclohexanecarboxylate hydrochloride
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting the central nervous system, where its structure can be modified to create compounds with specific therapeutic effects. Additionally, it is employed in research settings for the study of chemical reactions involving cyclohexane derivatives, aiding in the exploration of new synthetic pathways and the optimization of r

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals. It is particularly valuable in the development of drugs targeting the central nervous system, where its structure can be modified to create compounds with specific therapeutic effects. Additionally, it is employed in research settings for the study of chemical reactions involving cyclohexane derivatives, aiding in the exploration of new synthetic pathways and the optimization of reaction conditions. Its hydrochloride form enhances stability and solubility, making it easier to handle and incorporate into various chemical processes.

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