1-Methyl-3-((phenylthio)methyl)-1H-pyrazol-5-ol

≥90%

Reagent Code: #123878
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CAS Number 318234-24-1

science Other reagents with same CAS 318234-24-1

blur_circular Chemical Specifications

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Weight 220.29 g/mol
Formula C₁₁H₁₂N₂OS
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MDL Number MFCD00794867
inventory_2 Storage & Handling
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description Product Description

This compound, 1-Methyl-3-((phenylthio)methyl)-1H-pyrazol-5-ol, is utilized as a key intermediate in organic synthesis, particularly for developing bioactive chemicals in the pharmaceutical industry. Its structure, incorporating a pyrazole ring with a methyl substituent at N1, a (phenylthio)methyl group at C3, and a hydroxy group at C5, enables modifications to produce compounds with anti-inflammatory, antifungal, or enzyme-inhibitory activities. It serves as a building block for targeted drug discovery, including potential treatments for neurological disorders or cellular abnormalities. Additionally, it supports the synthesis of heterocyclic compounds essential in agrochemicals, dyes, pigments, and other specialty chemicals, leveraging its reactivity for diverse functionalized products.

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inventory 100mg
10-20 days ฿22,239.00

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1-Methyl-3-((phenylthio)methyl)-1H-pyrazol-5-ol
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This compound, 1-Methyl-3-((phenylthio)methyl)-1H-pyrazol-5-ol, is utilized as a key intermediate in organic synthesis, particularly for developing bioactive chemicals in the pharmaceutical industry. Its structure, incorporating a pyrazole ring with a methyl substituent at N1, a (phenylthio)methyl group at C3, and a hydroxy group at C5, enables modifications to produce compounds with anti-inflammatory, antifungal, or enzyme-inhibitory activities. It serves as a building block for targeted drug discovery,

This compound, 1-Methyl-3-((phenylthio)methyl)-1H-pyrazol-5-ol, is utilized as a key intermediate in organic synthesis, particularly for developing bioactive chemicals in the pharmaceutical industry. Its structure, incorporating a pyrazole ring with a methyl substituent at N1, a (phenylthio)methyl group at C3, and a hydroxy group at C5, enables modifications to produce compounds with anti-inflammatory, antifungal, or enzyme-inhibitory activities. It serves as a building block for targeted drug discovery, including potential treatments for neurological disorders or cellular abnormalities. Additionally, it supports the synthesis of heterocyclic compounds essential in agrochemicals, dyes, pigments, and other specialty chemicals, leveraging its reactivity for diverse functionalized products.

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