4-bromo-5-(bromomethyl)-1-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one

≥90%

Reagent Code: #197440
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CAS Number 5767-66-8

science Other reagents with same CAS 5767-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.03 g/mol
Formula C₁₁H₁₀Br₂N₂O
badge Registry Numbers
MDL Number MFCD00129260
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and anti-inflammatory properties. Its reactive bromomethyl group allows for easy functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as an alkylating agent in ring systems. Also utilized in the preparation of dyes and functional materials where halogenated pyrazolone derivatives enhance photostability and colorfastness.

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inventory 5mg
10-20 days ฿5,700.00

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4-bromo-5-(bromomethyl)-1-methyl-2-phenyl-2,3-dihydro-1H-pyrazol-3-one
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and anti-inflammatory properties. Its reactive bromomethyl group allows for easy functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as an alkylating agent in ring systems. Also utilized in the preparat

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and anti-inflammatory properties. Its reactive bromomethyl group allows for easy functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to act as an alkylating agent in ring systems. Also utilized in the preparation of dyes and functional materials where halogenated pyrazolone derivatives enhance photostability and colorfastness.

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