tert-Butyl (4-bromothiophen-3-yl)carbamate

95%

Reagent Code: #152735
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CAS Number 119485-57-3

science Other reagents with same CAS 119485-57-3

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inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of thiophene-based drug candidates. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules where the thiophene ring acts as a core scaffold. The tert-butyl carbamate (Boc) group ensures stability during reactions and can be easily removed under mild acidic conditions, making it ideal for use in peptide-like coupling and heterocyclic chemistry. Also utilized in the fabrication of organic semiconductors due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,290.00
inventory 250mg
10-20 days ฿13,920.00
inventory 1g
10-20 days ฿34,980.00
inventory 5g
10-20 days ฿124,440.00

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tert-Butyl (4-bromothiophen-3-yl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of thiophene-based drug candidates. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules where the thiophene ring acts as a core scaffold. The tert-butyl carbamate (Boc) group ensures stability during reactions and can be easily removed under mild acidic conditions, making it ideal for use in pepti

Used as an intermediate in pharmaceutical synthesis, particularly in the development of thiophene-based drug candidates. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules where the thiophene ring acts as a core scaffold. The tert-butyl carbamate (Boc) group ensures stability during reactions and can be easily removed under mild acidic conditions, making it ideal for use in peptide-like coupling and heterocyclic chemistry. Also utilized in the fabrication of organic semiconductors due to the electron-rich nature of the thiophene ring.

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