2,5-Dimethoxyphenyl isothiocyanate

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Reagent Code: #83226
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CAS Number 40532-06-7

science Other reagents with same CAS 40532-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.24 g/mol
Formula C₉H₉NO₂S
badge Registry Numbers
MDL Number MFCD00041059
thermostat Physical Properties
Melting Point 35-37 °C
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its isothiocyanate group is particularly valuable for creating thiourea derivatives, which are often explored for their biological activities, including antimicrobial and anticancer properties. Additionally, it is utilized in the development of dyes and pigments due to its ability to form stable covalent bonds with other molecules. In research, it is employed as a reagent for modifying proteins and peptides, aiding in the study of biochemical pathways and interactions. Its applications also extend to material science, where it is used to synthesize polymers with specific functional properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿990.00
inventory 5g
10-20 days ฿4,131.00
inventory 25g
10-20 days ฿16,191.00

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2,5-Dimethoxyphenyl isothiocyanate
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its isothiocyanate group is particularly valuable for creating thiourea derivatives, which are often explored for their biological activities, including antimicrobial and anticancer properties. Additionally, it is utilized in the development of dyes and pigments due to its ability to form stable covalent bonds with other molecules. In research, it is employed as

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its isothiocyanate group is particularly valuable for creating thiourea derivatives, which are often explored for their biological activities, including antimicrobial and anticancer properties. Additionally, it is utilized in the development of dyes and pigments due to its ability to form stable covalent bonds with other molecules. In research, it is employed as a reagent for modifying proteins and peptides, aiding in the study of biochemical pathways and interactions. Its applications also extend to material science, where it is used to synthesize polymers with specific functional properties.

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