(R)-1-(3-Chloro-4-methylphenyl)ethanamine hydrochloride

97%

Reagent Code: #230476
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CAS Number 856562-92-0

science Other reagents with same CAS 856562-92-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.11 g/mol
Formula C₉H₁₃Cl₂N
badge Registry Numbers
MDL Number MFCD16293365
thermostat Physical Properties
Boiling Point 223.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

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 compounds with central nervous system activity, including potential use in antidepressants or antipsychotics. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling selective formation of desired enantiomers in drug manufacturing. Also utilized in the preparation of intermediates for agrochemicals and bioactive molecules where specific stereochemistry is critical for activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,660.00
250mg
10-20 days ฿4,340.00
(R)-1-(3-Chloro-4-methylphenyl)ethanamine 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 compounds with central nervous system activity, including potential use in antidepressants or antipsychotics. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling selective formation of desired enantiomers in drug manufacturing. Also utilized in

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 compounds with central nervous system activity, including potential use in antidepressants or antipsychotics. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling selective formation of desired enantiomers in drug manufacturing. Also utilized in the preparation of intermediates for agrochemicals and bioactive molecules where specific stereochemistry is critical for activity.

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