N1,N2-Dimethylcyclohexane-1,2-diamine hydrochloride

≥95%

Reagent Code: #53063
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CAS Number 1956325-54-4

science Other reagents with same CAS 1956325-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.70 g/mol
Formula C₈H₁₉ClN₂
badge Registry Numbers
MDL Number MFCD21603997
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the production of pharmaceuticals and fine chemicals, helping to create compounds with specific stereochemistry. Additionally, it is employed in the development of catalysts for organic transformations, such as hydrogenation and carbon-carbon bond formation. Its application extends to research and development in academic and industrial laboratories, where it aids in the study of stereochemical outcomes in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,521.00
inventory 5g
10-20 days ฿4,509.00
inventory 250mg
10-20 days ฿765.00

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N1,N2-Dimethylcyclohexane-1,2-diamine hydrochloride
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the production of pharmaceuticals and fine chemicals, helping to create compounds with specific stereochemistry. Additionally, it is employed in the development of catalysts for organic transformations, such as hydrogenation and carbon-carbon bond formation. Its application extends to research and development in academic and in

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It plays a significant role in the production of pharmaceuticals and fine chemicals, helping to create compounds with specific stereochemistry. Additionally, it is employed in the development of catalysts for organic transformations, such as hydrogenation and carbon-carbon bond formation. Its application extends to research and development in academic and industrial laboratories, where it aids in the study of stereochemical outcomes in synthetic pathways.

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