Methyl 6-chloropyridazine-3-carboxylate

98%

Reagent Code: #205525
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CAS Number 65202-50-8

science Other reagents with same CAS 65202-50-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.57 g/mol
Formula C₆H₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD08694876
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 herbicides and plant growth regulators. Its structure allows for functionalization at multiple sites, making it valuable in agrochemical research for creating compounds with selective biological activity. It is also employed in the preparation of pyridazine-based derivatives that show potential in medicinal chemistry, including treatments targeting inflammatory and central nervous system disorders. The ester group facilitates coupling reactions, enabling the construction of complex molecules in drug discovery pipelines.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
5g
10-20 days ฿690.00
100g
10-20 days ฿10,690.00
500g
10-20 days ฿53,400.00
25g
10-20 days ฿2,690.00
Methyl 6-chloropyridazine-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for functionalization at multiple sites, making it valuable in agrochemical research for creating compounds with selective biological activity. It is also employed in the preparation of pyridazine-based derivatives that show potential in medicinal chemistry, including treatments targeting inflammatory and central nervous system disorders. The este

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure allows for functionalization at multiple sites, making it valuable in agrochemical research for creating compounds with selective biological activity. It is also employed in the preparation of pyridazine-based derivatives that show potential in medicinal chemistry, including treatments targeting inflammatory and central nervous system disorders. The ester group facilitates coupling reactions, enabling the construction of complex molecules in drug discovery pipelines.

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