Methyl 4-amino-3-formylbenzoate

≥95%

Reagent Code: #205631
fingerprint
CAS Number 841296-15-9

science Other reagents with same CAS 841296-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.17 g/mol
Formula C₉H₉NO₃
badge Registry Numbers
MDL Number MFCD16660047
thermostat Physical Properties
Melting Point 122-124 °C
Boiling Point 374.2±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.268±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) where the aldehyde and amine functional groups allow for further derivatization. Commonly employed in the preparation of heterocyclic compounds, including quinazolines and other nitrogen-containing rings, which are prevalent in medicinal chemistry. Also utilized in dye synthesis and organic synthesis research due to its bifunctional reactivity, enabling Schiff base formation or reduction reactions to produce amino alcohols or aminomethyl derivatives.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,760.00
250mg
10-20 days ฿2,560.00
1g
10-20 days ฿6,400.00
5g
10-20 days ฿19,200.00
25g
10-20 days ฿64,000.00
Methyl 4-amino-3-formylbenzoate
No image available

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) where the aldehyde and amine functional groups allow for further derivatization. Commonly employed in the preparation of heterocyclic compounds, including quinazolines and other nitrogen-containing rings, which are prevalent in medicinal chemistry. Also utilized in dye synthesis and organic synthesis research due to its bifunctional reactivity, enabli

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of active pharmaceutical ingredients (APIs) where the aldehyde and amine functional groups allow for further derivatization. Commonly employed in the preparation of heterocyclic compounds, including quinazolines and other nitrogen-containing rings, which are prevalent in medicinal chemistry. Also utilized in dye synthesis and organic synthesis research due to its bifunctional reactivity, enabling Schiff base formation or reduction reactions to produce amino alcohols or aminomethyl derivatives.

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...