(S)-2-Amino-1-phenylethanol

Standard for GC, ≥99.8%(GC)

Reagent Code: #232406
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CAS Number 56613-81-1

science Other reagents with same CAS 56613-81-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.18 g/mol
Formula C₈H₁₁NO
badge Registry Numbers
MDL Number MFCD00239405
thermostat Physical Properties
Melting Point 57-59 °C
Boiling Point 160 °C/17mm
inventory_2 Storage & Handling
Density 1.104±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in active pharmaceutical ingredients. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Additionally, it serves as an intermediate in the development of central nervous system agents and adrenergic receptor modulators.

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inventory 1g
10-20 days ฿12,600.00

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(S)-2-Amino-1-phenylethanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in active pharmaceutical ingredients. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Additionally, it serves as an intermediate in the development of central nervous system agents and adrenergic receptor

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomeric purity makes it valuable in asymmetric synthesis, where it helps control stereochemistry in active pharmaceutical ingredients. Also employed in the preparation of chiral ligands and catalysts for enantioselective reactions. Additionally, it serves as an intermediate in the development of central nervous system agents and adrenergic receptor modulators.

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