4-(2-Chloroethyl)-1H-pyrazole

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Reagent Code: #163922
label
Alias 4-Chloroethylpyrazole
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CAS Number 438475-37-7

science Other reagents with same CAS 438475-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.58 g/mol
Formula C₅H₇ClN₂
badge Registry Numbers
MDL Number MFCD08059907
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with biological activity. It serves in the preparation of central nervous system agents and has been explored in the creation of compounds with potential anticonvulsant, anti-inflammatory, and anticancer properties. Its reactive chloroethyl group allows for alkylation or chain extension in medicinal chemistry routes, making it valuable in building complex heterocyclic systems for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,000.00
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿4,510.00
inventory 5g
10-20 days ฿16,400.00
inventory 25g
10-20 days ฿52,980.00

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4-(2-Chloroethyl)-1H-pyrazole
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with biological activity. It serves in the preparation of central nervous system agents and has been explored in the creation of compounds with potential anticonvulsant, anti-inflammatory, and anticancer properties. Its reactive chloroethyl group allows for alkylation or chain extension in medicinal chemistry routes, making it valuable in building complex heterocyclic systems for drug disc

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of pyrazole-based drugs with biological activity. It serves in the preparation of central nervous system agents and has been explored in the creation of compounds with potential anticonvulsant, anti-inflammatory, and anticancer properties. Its reactive chloroethyl group allows for alkylation or chain extension in medicinal chemistry routes, making it valuable in building complex heterocyclic systems for drug discovery.

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