2,4,6-Trichloropyrimidine-5-carbaldehyde

97%

Reagent Code: #240336
label
Alias 2,4,6-Trichloro-5-formylpyrimidine
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CAS Number 50270-27-4

science Other reagents with same CAS 50270-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.43 g/mol
Formula C₅HCl₃N₂O
badge Registry Numbers
MDL Number MFCD02257700
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactive aldehyde and chlorine groups allow for selective modifications, enabling the construction of complex heterocyclic systems. Commonly employed in condensation and nucleophilic substitution reactions to introduce the pyrimidine scaffold into active ingredients. Also utilized in the preparation of dyes and functional materials due to its electron-deficient aromatic ring, which supports charge-transfer interactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿350.00
inventory 25g
10-20 days ฿1,530.00
inventory 100g
10-20 days ฿5,880.00

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2,4,6-Trichloropyrimidine-5-carbaldehyde
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactive aldehyde and chlorine groups allow for selective modifications, enabling the construction of complex heterocyclic systems. Commonly employed in condensation and nucleophilic substitution reactions to introduce the pyrimidine scaffold into active ingredients. Also utilized in the preparation of dyes and functional materials due to its electron-deficie

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its reactive aldehyde and chlorine groups allow for selective modifications, enabling the construction of complex heterocyclic systems. Commonly employed in condensation and nucleophilic substitution reactions to introduce the pyrimidine scaffold into active ingredients. Also utilized in the preparation of dyes and functional materials due to its electron-deficient aromatic ring, which supports charge-transfer interactions.

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