4-(5-Bromo-1,3,4-thiadiazol-2-yl)morpholine

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Reagent Code: #146164
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CAS Number 1341405-19-3

science Other reagents with same CAS 1341405-19-3

blur_circular Chemical Specifications

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Weight 250.12 g/mol
Formula C₆H₈BrN₃OS
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for antimicrobial, antiviral, and antitumor agents. The compound's structure, featuring a morpholine group and bromo substituent on the 1,3,4-thiadiazole ring, supports the development of bioactive molecules, particularly in heterocyclic chemistry. It is employed in structure-activity relationship (SAR) studies of pharmaceutical lead compounds and in the design of kinase inhibitors and other enzyme-targeted drugs due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions. Additionally, it serves as a reagent in group transfer reactions or carbon-carbon bond formation in multi-component synthesis. It also finds use in agrochemical research for developing new crop protection agents.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿2,350.00

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4-(5-Bromo-1,3,4-thiadiazol-2-yl)morpholine
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Used in pharmaceutical synthesis as an intermediate for antimicrobial, antiviral, and antitumor agents. The compound's structure, featuring a morpholine group and bromo substituent on the 1,3,4-thiadiazole ring, supports the development of bioactive molecules, particularly in heterocyclic chemistry. It is employed in structure-activity relationship (SAR) studies of pharmaceutical lead compounds and in the design of kinase inhibitors and other enzyme-targeted drugs due to its ability to interact with biol

Used in pharmaceutical synthesis as an intermediate for antimicrobial, antiviral, and antitumor agents. The compound's structure, featuring a morpholine group and bromo substituent on the 1,3,4-thiadiazole ring, supports the development of bioactive molecules, particularly in heterocyclic chemistry. It is employed in structure-activity relationship (SAR) studies of pharmaceutical lead compounds and in the design of kinase inhibitors and other enzyme-targeted drugs due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions. Additionally, it serves as a reagent in group transfer reactions or carbon-carbon bond formation in multi-component synthesis. It also finds use in agrochemical research for developing new crop protection agents.

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