5-Fluoro-2-methylphenyl Isothiocyanate

98%

Reagent Code: #77340
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CAS Number 175205-39-7

science Other reagents with same CAS 175205-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.20 g/mol
Formula C₈H₆FNS
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of various heterocyclic compounds. Its isothiocyanate group is particularly reactive, making it valuable for constructing thiourea derivatives, which are often explored for their potential biological activities. In medicinal chemistry, it is employed to develop novel pharmacophores, especially in the design of molecules with potential anticancer, antimicrobial, or anti-inflammatory properties. Additionally, it finds application in the synthesis of agrochemicals, contributing to the development of new pesticides or herbicides. Its unique structure also makes it a useful reagent in the study of chemical reactions and mechanisms, particularly those involving sulfur-containing compounds.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 97.5-100
Refractive Index (n20/D) 1.608-1.612
Density (20°C) 1.202-1.206
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 5g
10-20 days ฿2,331.00

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5-Fluoro-2-methylphenyl Isothiocyanate
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of various heterocyclic compounds. Its isothiocyanate group is particularly reactive, making it valuable for constructing thiourea derivatives, which are often explored for their potential biological activities. In medicinal chemistry, it is employed to develop novel pharmacophores, especially in the design of molecules with potential anticancer, antimicrobial, or anti-inflamma

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the preparation of various heterocyclic compounds. Its isothiocyanate group is particularly reactive, making it valuable for constructing thiourea derivatives, which are often explored for their potential biological activities. In medicinal chemistry, it is employed to develop novel pharmacophores, especially in the design of molecules with potential anticancer, antimicrobial, or anti-inflammatory properties. Additionally, it finds application in the synthesis of agrochemicals, contributing to the development of new pesticides or herbicides. Its unique structure also makes it a useful reagent in the study of chemical reactions and mechanisms, particularly those involving sulfur-containing compounds.

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