(R)-1-Mesitylethanaminehydrochloride

98%

Reagent Code: #232055
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CAS Number 1032153-84-6

science Other reagents with same CAS 1032153-84-6

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scatter_plot Molecular Information
Weight 199.72 g/mol
Formula C₁₁H₁₈ClN
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its bulky mesityl group enhances stereoselectivity in reactions such as catalytic hydrogenation and nucleophilic additions. Commonly employed in the preparation of chiral ligands and organocatalysts, enabling efficient synthesis of complex molecules with high optical purity. Also utilized in resolution processes to separate enantiomers due to its well-defined stereochemistry and crystalline properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,600.00
inventory 250mg
10-20 days ฿18,840.00
inventory 1g
10-20 days ฿46,250.00
(R)-1-Mesitylethanaminehydrochloride
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Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its bulky mesityl group enhances stereoselectivity in reactions such as catalytic hydrogenation and nucleophilic additions. Commonly employed in the preparation of chiral ligands and organocatalysts, enabling efficient synthesis of complex molecules with high optical purity. Also utilized in resolution processes to separate enantiomers due to its well-defined st

Used as a chiral building block in asymmetric synthesis, particularly in the pharmaceutical industry for developing enantiomerically pure drugs. Its bulky mesityl group enhances stereoselectivity in reactions such as catalytic hydrogenation and nucleophilic additions. Commonly employed in the preparation of chiral ligands and organocatalysts, enabling efficient synthesis of complex molecules with high optical purity. Also utilized in resolution processes to separate enantiomers due to its well-defined stereochemistry and crystalline properties.

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