(S)-3-Amino-4,4-diphenylbutanoic acid hydrochloride

≥95%

Reagent Code: #38453
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CAS Number 332062-01-8

science Other reagents with same CAS 332062-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.77 g/mol
Formula C₁₆H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD03092955
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. It is often employed in the development of medications for neurological disorders, such as epilepsy and chronic pain, where the resulting APIs interact with specific receptors in the brain. Additionally, its diphenyl moiety contributes to the creation of compounds with enhanced binding affinity and selectivity, making it a crucial component in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,825.00
inventory 250mg
10-20 days ฿7,659.00

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(S)-3-Amino-4,4-diphenylbutanoic acid hydrochloride
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This compound is primarily utilized in the pharmaceutical industry as a key chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. It is often employed in the development of medications for neurological disorders, such as epilepsy and chronic pain, where the resulting APIs interact with specific receptors in t

This compound is primarily utilized in the pharmaceutical industry as a key chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure drugs, particularly those targeting the central nervous system. It is often employed in the development of medications for neurological disorders, such as epilepsy and chronic pain, where the resulting APIs interact with specific receptors in the brain. Additionally, its diphenyl moiety contributes to the creation of compounds with enhanced binding affinity and selectivity, making it a crucial component in drug discovery and development processes.

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