(R)-4-(1-Aminoethyl)benzonitrile

95%

Reagent Code: #37658
fingerprint
CAS Number 210488-53-2

science Other reagents with same CAS 210488-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.1891 g/mol
Formula C₉H₁₀N₂
badge Registry Numbers
MDL Number MFCD09829185
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral drugs. Its structure, featuring a benzonitrile group and an aminoethyl moiety, makes it a valuable intermediate for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) drugs, where the (R)-enantiomer can provide enhanced efficacy or reduced side effects. Additionally, it serves as a building block in organic synthesis for constructing complex molecules with high enantiomeric purity, which is critical in drug discovery and development processes. Its applications also extend to agrochemical research, where it aids in the design of chiral pesticides and herbicides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,637.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-4-(1-Aminoethyl)benzonitrile
No image available

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral drugs. Its structure, featuring a benzonitrile group and an aminoethyl moiety, makes it a valuable intermediate for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) drugs, where the (R)-enantiomer can provide enhanced efficacy or red

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of chiral drugs. Its structure, featuring a benzonitrile group and an aminoethyl moiety, makes it a valuable intermediate for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) drugs, where the (R)-enantiomer can provide enhanced efficacy or reduced side effects. Additionally, it serves as a building block in organic synthesis for constructing complex molecules with high enantiomeric purity, which is critical in drug discovery and development processes. Its applications also extend to agrochemical research, where it aids in the design of chiral pesticides and herbicides.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...