2-Amino-4,6-difluorobenzaldehyde

98%

Reagent Code: #135989
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CAS Number 1260790-53-1

science Other reagents with same CAS 1260790-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.12 g/mol
Formula C₇H₅F₂NO
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde and amine functional groups allow for versatile reactivity, enabling Schiff base formation or reductive amination, which are common steps in drug construction. Also employed in the preparation of agrochemicals and specialty dyes due to its electron-withdrawing fluorine atoms and aromatic scaffold, which contribute to improved photostability and reactivity selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿3,300.00
100mg
10-20 days ฿7,960.00
250mg
10-20 days ฿12,770.00
1g
10-20 days ฿32,040.00
5g
10-20 days ฿78,600.00
2-Amino-4,6-difluorobenzaldehyde
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde and amine functional groups allow for versatile reactivity, enabling Schiff base formation or reductive amination, which are common steps in drug construction. Also employed in the preparation of agrochemicals and specialty dyes due to its electron-withdrawing fluor

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where fluorine substitution enhances metabolic stability and bioavailability. Its aldehyde and amine functional groups allow for versatile reactivity, enabling Schiff base formation or reductive amination, which are common steps in drug construction. Also employed in the preparation of agrochemicals and specialty dyes due to its electron-withdrawing fluorine atoms and aromatic scaffold, which contribute to improved photostability and reactivity selectivity.

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