3-Amino-5-bromo-2-chloropyridine

98%

Reagent Code: #134572
label
Alias 3-amino-5-bromo-2-chloropyridine
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CAS Number 588729-99-1

science Other reagents with same CAS 588729-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.46 g/mol
Formula C₅H₄BrClN₂
badge Registry Numbers
MDL Number MFCD02682092
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. It is also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of multiple reactive sites (amino, bromo, chloro groups) enables sequential coupling and substitution reactions, which are essential in building complex heterocyclic systems for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿148.50
5g
10-20 days ฿176.00
25g
10-20 days ฿1,430.00
100g
10-20 days ฿5,570.00
500g
10-20 days ฿27,280.00
3-Amino-5-bromo-2-chloropyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. It is also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of multiple reactive sites (amino, bromo, chloro groups) enables sequential coupling and s

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides and insecticides. It is also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. The presence of multiple reactive sites (amino, bromo, chloro groups) enables sequential coupling and substitution reactions, which are essential in building complex heterocyclic systems for drug discovery.

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