4-(4-Methylphenyl)-3-thiosemicarbazide

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Reagent Code: #118777
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CAS Number 13278-67-6

science Other reagents with same CAS 13278-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.26 g/mol
Formula C₈H₁₁N₃S
badge Registry Numbers
MDL Number MFCD00041302
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the preparation of various heterocyclic compounds, which are often explored for their potential biological activities. Researchers have shown interest in its use for developing antimicrobial, antiviral, and anticancer agents due to its thiosemicarbazide moiety, which is known to exhibit significant pharmacological properties. Additionally, it is employed in the synthesis of coordination complexes with metals, which are studied for their potential applications in catalysis and material science. Its role in the development of chemosensors for detecting metal ions in environmental and biological samples is also noteworthy.

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Test Parameter Specification
Purity (%) 96.5-100
Melting Point 132-136°C
Appearance White Crystalline Powder

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inventory 5g
10-20 days ฿2,988.00

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4-(4-Methylphenyl)-3-thiosemicarbazide
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This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the preparation of various heterocyclic compounds, which are often explored for their potential biological activities. Researchers have shown interest in its use for developing antimicrobial, antiviral, and anticancer agents due to its thiosemicarbazide moiety, which is known to exhibit significant pharmacological properties. Additionally, it is employed in the synthesis of co

This compound is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the preparation of various heterocyclic compounds, which are often explored for their potential biological activities. Researchers have shown interest in its use for developing antimicrobial, antiviral, and anticancer agents due to its thiosemicarbazide moiety, which is known to exhibit significant pharmacological properties. Additionally, it is employed in the synthesis of coordination complexes with metals, which are studied for their potential applications in catalysis and material science. Its role in the development of chemosensors for detecting metal ions in environmental and biological samples is also noteworthy.

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