(R)-4-(1-Aminoethyl)-3-chlorobenzonitrile hydrochloride

95%

Reagent Code: #229215
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CAS Number 2703746-26-1

science Other reagents with same CAS 2703746-26-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.1 g/mol
Formula C₉H₁₀Cl₂N₂
badge Registry Numbers
MDL Number MFCD32670695
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. Its chiral amine functionality allows for stereoselective reactions, making it valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized in research settings for the preparation of structurally complex molecules requiring high enantiomeric purity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿19,040.00
(R)-4-(1-Aminoethyl)-3-chlorobenzonitrile hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. Its chiral amine functionality allows for stereoselective reactions, making it valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized in research settings for the preparatio

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. Its chiral amine functionality allows for stereoselective reactions, making it valuable in asymmetric synthesis. Commonly employed in the development of active pharmaceutical ingredients (APIs) where the (R)-enantiomer contributes to desired biological activity. Also utilized in research settings for the preparation of structurally complex molecules requiring high enantiomeric purity.

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