Rel-(1R,4R)-4-(4-(Cyclopropylmethyl)Piperazin-1-Yl)Cyclohexan-1-Amine Tris(4-Methylbenzenesulfonate)

98%

Reagent Code: #231528
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CAS Number 1373498-25-9

science Other reagents with same CAS 1373498-25-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 753.99 g/mol
Formula C₃₅H₅₁N₃O₉S₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Its structure, featuring a piperazine moiety and amine group, supports the development of central nervous system agents, particularly those targeting neurological and psychiatric disorders such as depression, anxiety, or schizophrenia. The compound's stereochemistry (rel-(1R,4R)) and functional groups make it valuable in optimizing drug candidates for improved binding affinity to brain receptors and metabolic stability. The tris(4-methylbenzenesulfonate) (tosylate) salt form enhances stability and water solubility, making it suitable for formulations requiring efficient absorption. It is also employed in structure-activity relationship (SAR) studies to enhance potency and selectivity of new therapeutic molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,500.00
Rel-(1R,4R)-4-(4-(Cyclopropylmethyl)Piperazin-1-Yl)Cyclohexan-1-Amine Tris(4-Methylbenzenesulfonate)
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Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Its structure, featuring a piperazine moiety and amine group, supports the development of central nervous system agents, particularly those targeting neurological and psychiatric disorders such as depression, anxiety, or schizophrenia. The compound's stereochemistry (rel-(1R,4R)) and functional groups make it valuable in optimizing drug candidates for improved binding affinity to brain receptor

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds. Its structure, featuring a piperazine moiety and amine group, supports the development of central nervous system agents, particularly those targeting neurological and psychiatric disorders such as depression, anxiety, or schizophrenia. The compound's stereochemistry (rel-(1R,4R)) and functional groups make it valuable in optimizing drug candidates for improved binding affinity to brain receptors and metabolic stability. The tris(4-methylbenzenesulfonate) (tosylate) salt form enhances stability and water solubility, making it suitable for formulations requiring efficient absorption. It is also employed in structure-activity relationship (SAR) studies to enhance potency and selectivity of new therapeutic molecules.

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