cis-4-Methylcyclohexanamine hydrochloride

98%

Reagent Code: #123395
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CAS Number 33483-66-8

science Other reagents with same CAS 33483-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.66 g/mol
Formula C₇H₁₆ClN
badge Registry Numbers
MDL Number MFCD09991703
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical industry. It serves as an intermediate in the production of various drugs, including those targeting neurological and cardiovascular conditions. The compound's structure allows it to act as a chiral precursor, aiding in the creation of enantiomerically pure substances. Additionally, it is employed in research and development for studying receptor interactions and biochemical pathways. Its hydrochloride form enhances stability and solubility, making it suitable for laboratory and industrial applications.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,260.00
inventory 1g
10-20 days ฿8,580.00
inventory 250mg
10-20 days ฿3,370.00

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cis-4-Methylcyclohexanamine hydrochloride
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Used in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical industry. It serves as an intermediate in the production of various drugs, including those targeting neurological and cardiovascular conditions. The compound's structure allows it to act as a chiral precursor, aiding in the creation of enantiomerically pure substances. Additionally, it is employed in research and development for studying receptor interactions and biochemical pathways. Its hydrochl

Used in organic synthesis as a building block for more complex molecules, particularly in the pharmaceutical industry. It serves as an intermediate in the production of various drugs, including those targeting neurological and cardiovascular conditions. The compound's structure allows it to act as a chiral precursor, aiding in the creation of enantiomerically pure substances. Additionally, it is employed in research and development for studying receptor interactions and biochemical pathways. Its hydrochloride form enhances stability and solubility, making it suitable for laboratory and industrial applications.

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