2-(Methylamino)benzaldehyde

96%

Reagent Code: #206479
fingerprint
CAS Number 7755-70-6

science Other reagents with same CAS 7755-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.16 g/mol
Formula C₈H₉NO
badge Registry Numbers
MDL Number MFCD19216814
thermostat Physical Properties
Boiling Point 260.7°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of active ingredients requiring substituted benzaldehyde derivatives. Commonly employed in the development of dyes and fluorescent compounds due to its reactive aldehyde and amine functional groups. Also utilized in organic research for building heterocyclic compounds such as indoles and quinazolines, which are important scaffolds in medicinal chemistry. Its structure supports condensation reactions, making it valuable in the preparation of Schiff bases and other imine-based derivatives for biological evaluation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿660.00
inventory 250mg
10-20 days ฿1,480.00
inventory 1g
10-20 days ฿5,770.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(Methylamino)benzaldehyde
No image available

Used in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of active ingredients requiring substituted benzaldehyde derivatives. Commonly employed in the development of dyes and fluorescent compounds due to its reactive aldehyde and amine functional groups. Also utilized in organic research for building heterocyclic compounds such as indoles and quinazolines, which are important scaffolds in medicinal chemistry. Its structure supports condensation reacti

Used in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of active ingredients requiring substituted benzaldehyde derivatives. Commonly employed in the development of dyes and fluorescent compounds due to its reactive aldehyde and amine functional groups. Also utilized in organic research for building heterocyclic compounds such as indoles and quinazolines, which are important scaffolds in medicinal chemistry. Its structure supports condensation reactions, making it valuable in the preparation of Schiff bases and other imine-based derivatives for biological evaluation.

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...