4-Chloro-2-(1H-pyrazol-3-yl)phenol

98%

Reagent Code: #161345
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CAS Number 18704-67-1

science Other reagents with same CAS 18704-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.62 g/mol
Formula C₉H₇ClN₂O
badge Registry Numbers
MDL Number MFCD00209566
thermostat Physical Properties
Melting Point 157.0-161.0°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the development of strobilurin-class active ingredients. It contributes to the formation of compounds with strong antifungal activity against a broad spectrum of plant pathogens, including powdery mildews, rusts, and leaf spots. Its structure enables effective binding to fungal mitochondrial respiration sites, disrupting energy production and leading to pathogen death. Also investigated for use in pharmaceutical research due to the bioactive potential of pyrazole-containing molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿690.00
1g
10-20 days ฿2,460.00
5g
10-20 days ฿9,290.00
4-Chloro-2-(1H-pyrazol-3-yl)phenol
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Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the development of strobilurin-class active ingredients. It contributes to the formation of compounds with strong antifungal activity against a broad spectrum of plant pathogens, including powdery mildews, rusts, and leaf spots. Its structure enables effective binding to fungal mitochondrial respiration sites, disrupting energy production and leading to pathogen death. Also investigated for use in pharmaceutical resea

Used as a key intermediate in the synthesis of agricultural fungicides, particularly in the development of strobilurin-class active ingredients. It contributes to the formation of compounds with strong antifungal activity against a broad spectrum of plant pathogens, including powdery mildews, rusts, and leaf spots. Its structure enables effective binding to fungal mitochondrial respiration sites, disrupting energy production and leading to pathogen death. Also investigated for use in pharmaceutical research due to the bioactive potential of pyrazole-containing molecules.

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