(R)-4-Chloro-2,3-dihydro-1H-inden-1-amine hydrochloride

98%

Reagent Code: #231044
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CAS Number 1637453-69-0

science Other reagents with same CAS 1637453-69-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.098 g/mol
Formula C₉H₁₁Cl₂N
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MDL Number MFCD26585548
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its enantiomeric purity makes it valuable for developing active ingredients where stereochemistry impacts drug efficacy and safety. Commonly employed in asymmetric synthesis routes to ensure high optical purity of final drug substances. Also utilized in the preparation of catalysts and ligands for stereoselective reactions in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,790.00
inventory 250mg
10-20 days ฿6,680.00

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(R)-4-Chloro-2,3-dihydro-1H-inden-1-amine hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its enantiomeric purity makes it valuable for developing active ingredients where stereochemistry impacts drug efficacy and safety. Commonly employed in asymmetric synthesis routes to ensure high optical purity of final drug substances. Also utilized in the preparation of catalysts and ligands for stereoselective

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its enantiomeric purity makes it valuable for developing active ingredients where stereochemistry impacts drug efficacy and safety. Commonly employed in asymmetric synthesis routes to ensure high optical purity of final drug substances. Also utilized in the preparation of catalysts and ligands for stereoselective reactions in medicinal chemistry research.

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