(R)-2-Amino-3-(benzyloxy)propan-1-ol hydrochloride

≥95%

Reagent Code: #113534
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CAS Number 58577-95-0

science Other reagents with same CAS 58577-95-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.69 g/mol
Formula C₁₀H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD04112476
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in the synthesis of chiral molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral nature allows for the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is utilized in organic chemistry for the preparation of complex molecules, aiding in the study of stereochemistry and reaction mechanisms. Its benzyloxy group provides a protective functionality, making it valuable in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,629.00
inventory 1g
10-20 days ฿4,077.00
inventory 5g
10-20 days ฿15,435.00
inventory 10g
10-20 days ฿22,725.00

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(R)-2-Amino-3-(benzyloxy)propan-1-ol hydrochloride
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This compound is primarily used in the synthesis of chiral molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral nature allows for the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is utilized in organic chemistry for the preparation of complex molecules, aiding in t

This compound is primarily used in the synthesis of chiral molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral nature allows for the development of enantiomerically pure drugs, enhancing their efficacy and reducing side effects. Additionally, it is utilized in organic chemistry for the preparation of complex molecules, aiding in the study of stereochemistry and reaction mechanisms. Its benzyloxy group provides a protective functionality, making it valuable in multi-step synthetic processes.

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