(R)-2-(1-Aminoethyl)phenol

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Reagent Code: #37474
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CAS Number 123983-05-1

science Other reagents with same CAS 123983-05-1

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Weight 137.1790 g/mol
Formula C₈H₁₁NO
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MDL Number MFCD06761853
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(R)-2-(1-Aminoethyl)phenol is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where its chiral center plays a critical role in ensuring the desired biological activity. This compound is often employed in the development of beta-blockers and other cardiovascular medications, where stereochemistry is crucial for efficacy and safety. Additionally, it finds applications in asymmetric synthesis, aiding in the creation of complex molecules with high optical purity. Its versatility also extends to agrochemical research, where it contributes to the development of chiral pesticides and herbicides.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,890.00
inventory 100mg
10-20 days ฿2,090.00
inventory 1g
10-20 days ฿9,440.00
inventory 5g
10-20 days ฿36,320.00

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(R)-2-(1-Aminoethyl)phenol
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(R)-2-(1-Aminoethyl)phenol is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where its chiral center plays a critical role in ensuring the desired biological activity. This compound is often employed in the development of beta-blockers and other cardiovascular medications, where stereochemistry is crucial for efficacy and safety. Additionally, it finds applications in a

(R)-2-(1-Aminoethyl)phenol is primarily utilized in the synthesis of chiral compounds, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of enantiomerically pure drugs, where its chiral center plays a critical role in ensuring the desired biological activity. This compound is often employed in the development of beta-blockers and other cardiovascular medications, where stereochemistry is crucial for efficacy and safety. Additionally, it finds applications in asymmetric synthesis, aiding in the creation of complex molecules with high optical purity. Its versatility also extends to agrochemical research, where it contributes to the development of chiral pesticides and herbicides.

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