(R)-1-(3-Chlorophenyl)propan-1-amine hydrochloride

95%

Reagent Code: #37327
fingerprint
CAS Number 1168139-40-9

science Other reagents with same CAS 1168139-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.11222 g/mol
Formula C₉H₁₃Cl₂N
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a chiral intermediate in the production of drugs targeting the central nervous system, such as antidepressants and stimulants, due to its structural similarity to phenethylamine derivatives. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in organic chemistry studies to explore stereoselective reactions and asymmetric synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,623.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-1-(3-Chlorophenyl)propan-1-amine hydrochloride
No image available

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a chiral intermediate in the production of drugs targeting the central nervous system, such as antidepressants and stimulants, due to its structural similarity to phenethylamine derivatives. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for enhancing drug efficacy and reducing side effects.

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a chiral intermediate in the production of drugs targeting the central nervous system, such as antidepressants and stimulants, due to its structural similarity to phenethylamine derivatives. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in organic chemistry studies to explore stereoselective reactions and asymmetric synthesis.

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...