N-(2-phenylethyl)benzamide

95%

Reagent Code: #218399
fingerprint
CAS Number 3278-14-6

science Other reagents with same CAS 3278-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.2857 g/mol
Formula C₁₅H₁₅NO
badge Registry Numbers
MDL Number MFCD00441484
thermostat Physical Properties
Melting Point 117-118 °C
Boiling Point 439 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of amide-based molecules with potential neurological or anti-inflammatory activity. Due to its structural similarity to phenethylamine derivatives, it is also explored in medicinal chemistry for designing compounds that can cross the blood-brain barrier. Additionally, it finds use in research settings for studying amide bond reactivity and conformational behavior in aromatic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿970.00
inventory 25g
10-20 days ฿2,030.00
inventory 100g
10-20 days ฿7,950.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(2-phenylethyl)benzamide
No image available

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of amide-based molecules with potential neurological or anti-inflammatory activity. Due to its structural similarity to phenethylamine derivatives, it is also explored in medicinal chemistry for designing compounds that can cross the blood-brain barrier. Additionally, it finds use in research settings for studying amide bond rea

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. It serves as a building block in the development of amide-based molecules with potential neurological or anti-inflammatory activity. Due to its structural similarity to phenethylamine derivatives, it is also explored in medicinal chemistry for designing compounds that can cross the blood-brain barrier. Additionally, it finds use in research settings for studying amide bond reactivity and conformational behavior in aromatic systems.

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...