(S)-5-(Trifluoromethyl)-2,3-dihydro-1H-inden-1-amine hydrochloride

95%

Reagent Code: #233375
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CAS Number 2514660-75-2

science Other reagents with same CAS 2514660-75-2

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Weight 237.65 g/mol
Formula C₁₀H₁₁ClF₃N
badge Registry Numbers
MDL Number MFCD26585415
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 (CNS) active agents. Its chiral amine structure makes it valuable for asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy and safety. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter activity. Also utilized in the preparation of enzyme inhibitors and receptor modulators in medicinal chemistry research. Its trifluoromethyl group enhances metabolic stability and lipophilicity, improving drug bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿44,080.00

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(S)-5-(Trifluoromethyl)-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 (CNS) active agents. Its chiral amine structure makes it valuable for asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy and safety. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter activity. Also utilized in the p

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 (CNS) active agents. Its chiral amine structure makes it valuable for asymmetric synthesis, where stereochemistry plays a critical role in drug efficacy and safety. Commonly employed in the development of antidepressants and anxiolytic drugs due to its ability to influence neurotransmitter activity. Also utilized in the preparation of enzyme inhibitors and receptor modulators in medicinal chemistry research. Its trifluoromethyl group enhances metabolic stability and lipophilicity, improving drug bioavailability.

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