(S)-1-(2,3-Dihydro-1H-inden-4-yl)ethan-1-amine hydrochloride

95%

Reagent Code: #233423
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CAS Number 2703746-20-5

science Other reagents with same CAS 2703746-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.7 g/mol
Formula C₁₁H₁₆ClN
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MDL Number MFCD34186987
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

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 is critical for achieving desired biological activity and minimizing side effects in final drug products. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization. Also utilized in the development of radiolabeled compounds for receptor binding studies due to its structural stability and specificity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,590.00
inventory 100mg
10-20 days ฿21,820.00

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(S)-1-(2,3-Dihydro-1H-inden-4-yl)ethan-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 is critical for achieving desired biological activity and minimizing side effects in final drug products. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization. Also utilized in the development of radiolabeled compounds for r

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 is critical for achieving desired biological activity and minimizing side effects in final drug products. Commonly employed in asymmetric synthesis routes where the amine group serves as a handle for further functionalization. Also utilized in the development of radiolabeled compounds for receptor binding studies due to its structural stability and specificity.

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