(2S,3S)-3-Amino-1-chloro-4-phenylbutan-2-ol hydrochloride

95%

Reagent Code: #36541
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CAS Number 166987-16-2

science Other reagents with same CAS 166987-16-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.1382 g/mol
Formula C₁₀H₁₅Cl₂NO
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of β-blockers, which are drugs used to manage cardiovascular conditions such as hypertension, arrhythmias, and heart failure. Its stereospecific structure makes it a valuable chiral building block in asymmetric synthesis, ensuring the production of enantiomerically pure compounds. Additionally, it finds application in research and development for studying receptor interactions and drug mechanisms due to its structural similarity to biologically active molecules. Its hydrochloride form enhances solubility, making it suitable for various experimental and industrial processes.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100%
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,032.00
inventory 25g
10-20 days ฿8,082.00
inventory 1g
10-20 days ฿1,332.00

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(2S,3S)-3-Amino-1-chloro-4-phenylbutan-2-ol hydrochloride
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of β-blockers, which are drugs used to manage cardiovascular conditions such as hypertension, arrhythmias, and heart failure. Its stereospecific structure makes it a valuable chiral building block in asymmetric synthesis, ensuring the production of enantiomerically pure compounds. Additionally, it finds application in research and development for studying receptor interactions and drug mec

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of β-blockers, which are drugs used to manage cardiovascular conditions such as hypertension, arrhythmias, and heart failure. Its stereospecific structure makes it a valuable chiral building block in asymmetric synthesis, ensuring the production of enantiomerically pure compounds. Additionally, it finds application in research and development for studying receptor interactions and drug mechanisms due to its structural similarity to biologically active molecules. Its hydrochloride form enhances solubility, making it suitable for various experimental and industrial processes.

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