5-Bromonicotinohydrazide

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Reagent Code: #149832
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CAS Number 112193-41-6

science Other reagents with same CAS 112193-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.04 g/mol
Formula C₆H₆BrN₃O
badge Registry Numbers
MDL Number MFCD00173916
inventory_2 Storage & Handling
Storage 2-8℃, away from light, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for hydrazide-based drugs due to its ability to form stable derivatives with carbonyl compounds. Also employed in the preparation of heterocyclic compounds like 1,3,4-oxadiazoles and 1,3,4-thiadiazoles, which exhibit biological activity. Its bromine functionality allows for further cross-coupling reactions, making it valuable in medicinal chemistry research for structure-activity relationship studies.

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Test Parameter Specification
Appearance Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,580.00
inventory 25g
10-20 days ฿4,152.00

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5-Bromonicotinohydrazide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for hydrazide-based drugs due to its ability to form stable derivatives with carbonyl compounds. Also employed in the preparation of heterocyclic compounds like 1,3,4-oxadiazoles and 1,3,4-thiadiazoles, which exhibit biological activity. Its bromine functionality allows for further cross-coupling reactions, making it valuable in me

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for hydrazide-based drugs due to its ability to form stable derivatives with carbonyl compounds. Also employed in the preparation of heterocyclic compounds like 1,3,4-oxadiazoles and 1,3,4-thiadiazoles, which exhibit biological activity. Its bromine functionality allows for further cross-coupling reactions, making it valuable in medicinal chemistry research for structure-activity relationship studies.

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