2,5-Dimethylphenylisothiocyanate

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Reagent Code: #179334
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CAS Number 19241-15-7

science Other reagents with same CAS 19241-15-7

blur_circular Chemical Specifications

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Weight 163.24 g/mol
Formula C₉H₉NS
badge Registry Numbers
MDL Number MFCD00046798
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into complex molecules. It is especially valuable in the preparation of thiourea derivatives, which are important intermediates in pharmaceuticals and agrochemicals. Its aromatic structure with methyl substituents enhances reactivity and selectivity in coupling reactions. Commonly employed in the development of bioactive compounds, including kinase inhibitors and receptor antagonists. Also utilized in chemical biology for labeling and modifying biomolecules due to the selective reactivity of the isothiocyanate group with amines. Its stability and ease of handling make it suitable for use in both laboratory-scale and industrial processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,210.00
inventory 25g
10-20 days ฿11,850.00
inventory 5g
10-20 days ฿2,910.00

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2,5-Dimethylphenylisothiocyanate
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Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into complex molecules. It is especially valuable in the preparation of thiourea derivatives, which are important intermediates in pharmaceuticals and agrochemicals. Its aromatic structure with methyl substituents enhances reactivity and selectivity in coupling reactions. Commonly employed in the development of bioactive compounds, including kinase inhibitors and receptor antagon

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into complex molecules. It is especially valuable in the preparation of thiourea derivatives, which are important intermediates in pharmaceuticals and agrochemicals. Its aromatic structure with methyl substituents enhances reactivity and selectivity in coupling reactions. Commonly employed in the development of bioactive compounds, including kinase inhibitors and receptor antagonists. Also utilized in chemical biology for labeling and modifying biomolecules due to the selective reactivity of the isothiocyanate group with amines. Its stability and ease of handling make it suitable for use in both laboratory-scale and industrial processes.

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