3-(tert-Butoxycarbonyl)phenyl isothiocyanate

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Reagent Code: #78650
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CAS Number 486415-53-6

science Other reagents with same CAS 486415-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.30 g/mol
Formula C₁₂H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD03453225
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into organic molecules. It is particularly valuable in the preparation of thiourea derivatives, which are widely utilized in pharmaceutical research for developing drugs with potential therapeutic properties. Additionally, it finds application in the synthesis of heterocyclic compounds, which are important in the production of agrochemicals and dyes. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity, making it a versatile tool in peptide chemistry and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,740.00
inventory 1g
10-20 days ฿21,591.00

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3-(tert-Butoxycarbonyl)phenyl isothiocyanate
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Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into organic molecules. It is particularly valuable in the preparation of thiourea derivatives, which are widely utilized in pharmaceutical research for developing drugs with potential therapeutic properties. Additionally, it finds application in the synthesis of heterocyclic compounds, which are important in the production of agrochemicals and dyes. Its tert-butoxycarbonyl (Boc)

Used primarily in organic synthesis, this compound serves as a key reagent for introducing the isothiocyanate functional group into organic molecules. It is particularly valuable in the preparation of thiourea derivatives, which are widely utilized in pharmaceutical research for developing drugs with potential therapeutic properties. Additionally, it finds application in the synthesis of heterocyclic compounds, which are important in the production of agrochemicals and dyes. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity, making it a versatile tool in peptide chemistry and material science.

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