(S)-1-(5-Chloro-2-methylphenyl)ethan-1-amine hydrochloride

95%

Reagent Code: #233213
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CAS Number 2703746-03-4

science Other reagents with same CAS 2703746-03-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.11 g/mol
Formula C₉H₁₃Cl₂N
badge Registry Numbers
MDL Number MFCD34187010
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of biologically active molecules, especially in central nervous system agents and anti-inflammatory drugs. Commonly employed in asymmetric synthesis due to its stereochemical stability and reactivity in coupling reactions. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where regioselectivity and enantioselectivity are critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,020.00
inventory 250mg
10-20 days ฿35,950.00
inventory 1g
10-20 days ฿89,780.00
(S)-1-(5-Chloro-2-methylphenyl)ethan-1-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of biologically active molecules, especially in central nervous system agents and anti-inflammatory drugs. Commonly employed in asymmetric synthesis due to its stereochemical stability and reactivity in coupling reactions. Also utilized in the preparation of intermediates for agrochemicals a

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of biologically active molecules, especially in central nervous system agents and anti-inflammatory drugs. Commonly employed in asymmetric synthesis due to its stereochemical stability and reactivity in coupling reactions. Also utilized in the preparation of intermediates for agrochemicals and specialty chemicals where regioselectivity and enantioselectivity are critical.

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