(R)-(−)-2-Amino-1-pentanol

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Reagent Code: #56802
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CAS Number 80696-30-6

science Other reagents with same CAS 80696-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 103.16 g/mol
Formula C₅H₁₃NO
badge Registry Numbers
MDL Number MFCD02683228
thermostat Physical Properties
Melting Point 44-48°C
Boiling Point 195.6°C
inventory_2 Storage & Handling
Density 0.915 g/mL
Storage room temperature, dry

description Product Description

(R)-(−)-2-Amino-1-pentanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in the development of optically active compounds, particularly in the production of drugs where specific stereochemistry is crucial for biological activity. It serves as an intermediate in the synthesis of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Additionally, it is employed in the preparation of chiral ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. Its application extends to the field of agrochemicals, where it contributes to the creation of herbicides and pesticides with improved efficacy and reduced environmental impact.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿58,320.00

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(R)-(−)-2-Amino-1-pentanol
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(R)-(−)-2-Amino-1-pentanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in the development of optically active compounds, particularly in the production of drugs where specific stereochemistry is crucial for biological activity. It serves as an intermediate in the synthesis of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Additionally

(R)-(−)-2-Amino-1-pentanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals and fine chemicals. Its enantiomeric purity makes it valuable in the development of optically active compounds, particularly in the production of drugs where specific stereochemistry is crucial for biological activity. It serves as an intermediate in the synthesis of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Additionally, it is employed in the preparation of chiral ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. Its application extends to the field of agrochemicals, where it contributes to the creation of herbicides and pesticides with improved efficacy and reduced environmental impact.

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