(R)-()-4-Methoxy-α-methylbenzylamine

Standard for GC, ≥99.8%(GC)

Reagent Code: #228570
fingerprint
CAS Number 22038-86-4

science Other reagents with same CAS 22038-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
badge Registry Numbers
MDL Number MFCD00671659
thermostat Physical Properties
Melting Point <-20 °C
Boiling Point 65 °C/0.4mm
inventory_2 Storage & Handling
Density 1.024 g/mL at 20 °C(lit.)
Storage Room temperature, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Commonly employed in asymmetric synthesis due to its ability to act as a chiral auxiliary or resolving agent. Widely applied in the development of central nervous system drugs, including antidepressants and stimulants, where the (R)-enantiomer provides desired biological activity. Also utilized in the preparation of agrochemicals and fine chemicals where stereochemistry plays a critical role in efficacy. Its methoxy and amine functional groups allow for easy derivatization, making it valuable in medicinal chemistry research and process development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-()-4-Methoxy-α-methylbenzylamine
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Commonly employed in asymmetric synthesis due to its ability to act as a chiral auxiliary or resolving agent. Widely applied in the development of central nervous system drugs, including antidepressants and stimulants, where the (R)-enantiomer provides desired biological activity. Also utilized in the preparation of agrochemicals and

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients requiring high enantiomeric purity. Commonly employed in asymmetric synthesis due to its ability to act as a chiral auxiliary or resolving agent. Widely applied in the development of central nervous system drugs, including antidepressants and stimulants, where the (R)-enantiomer provides desired biological activity. Also utilized in the preparation of agrochemicals and fine chemicals where stereochemistry plays a critical role in efficacy. Its methoxy and amine functional groups allow for easy derivatization, making it valuable in medicinal chemistry research and process development.

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...