(R)-2-Amino-2-(2-bromophenyl)ethanol

95%

Reagent Code: #37539
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CAS Number 1213220-84-8

science Other reagents with same CAS 1213220-84-8

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Weight 216.0751 g/mol
Formula C₈H₁₀BrNO
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MDL Number MFCD09253606
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This compound is primarily utilized in the synthesis of chiral pharmaceuticals and fine chemicals due to its enantiomeric purity and structural properties. It serves as a key intermediate in the production of β-adrenergic receptor antagonists, which are widely used in treating cardiovascular diseases such as hypertension and arrhythmias. Additionally, its bromophenyl group makes it valuable in cross-coupling reactions, enabling the construction of complex organic molecules in medicinal chemistry. The compound is also employed in research for developing new asymmetric catalysts, enhancing the efficiency of stereoselective reactions.

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inventory 100mg
10-20 days ฿14,337.00

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(R)-2-Amino-2-(2-bromophenyl)ethanol
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This compound is primarily utilized in the synthesis of chiral pharmaceuticals and fine chemicals due to its enantiomeric purity and structural properties. It serves as a key intermediate in the production of β-adrenergic receptor antagonists, which are widely used in treating cardiovascular diseases such as hypertension and arrhythmias. Additionally, its bromophenyl group makes it valuable in cross-coupling reactions, enabling the construction of complex organic molecules in medicinal chemistry. The com

This compound is primarily utilized in the synthesis of chiral pharmaceuticals and fine chemicals due to its enantiomeric purity and structural properties. It serves as a key intermediate in the production of β-adrenergic receptor antagonists, which are widely used in treating cardiovascular diseases such as hypertension and arrhythmias. Additionally, its bromophenyl group makes it valuable in cross-coupling reactions, enabling the construction of complex organic molecules in medicinal chemistry. The compound is also employed in research for developing new asymmetric catalysts, enhancing the efficiency of stereoselective reactions.

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