1-methyl-1H-pyrazole-5-carbaldehyde

≥95%

Reagent Code: #193879
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CAS Number 27258-33-9

science Other reagents with same CAS 27258-33-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 110.11 g/mol
Formula C₅H₆N₂O
badge Registry Numbers
MDL Number MFCD03419801
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 active pharmaceutical ingredients (APIs) with anti-inflammatory, antiviral, and anticancer properties. Its aldehyde functional group allows for easy modification, enabling the formation of imines, oximes, and other derivatives useful in drug discovery. Commonly employed in agrochemical research for designing new pesticides and herbicides due to its heterocyclic structure, which enhances bioavailability and target specificity. Also utilized in the preparation of fluorescent probes and dyes, where the pyrazole ring contributes to photostability and emission properties. Frequently appears in combinatorial chemistry and high-throughput screening libraries for identifying novel bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿460.00
inventory 5g
10-20 days ฿1,460.00
inventory 100g
10-20 days ฿21,360.00
inventory 25g
10-20 days ฿5,700.00

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1-methyl-1H-pyrazole-5-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory, antiviral, and anticancer properties. Its aldehyde functional group allows for easy modification, enabling the formation of imines, oximes, and other derivatives useful in drug discovery. Commonly employed in agrochemical research for designing new pesticides and herbicides due to its heterocyclic structure, which enhances bioavailability and target specificity. Also utilized in the preparation of fluorescent probes and dyes, where the pyrazole ring contributes to photostability and emission properties. Frequently appears in combinatorial chemistry and high-throughput screening libraries for identifying novel bioactive compounds.
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