2-Bromothiobenzamide

97%

Reagent Code: #149537
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CAS Number 30216-44-5

science Other reagents with same CAS 30216-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.1 g/mol
Formula C₇H₆BrNS
badge Registry Numbers
MDL Number MFCD04973314
thermostat Physical Properties
Melting Point 82 - 86 ℃
Boiling Point 307 ℃ at 760mmHg
inventory_2 Storage & Handling
Density 1.634 g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals and agrochemicals due to its reactivity in cyclization reactions. Commonly employed in the synthesis of thiazoles and benzothiazoles, which are key scaffolds in medicinal chemistry. Also utilized in the formation of bioactive molecules and functional materials through palladium-catalyzed coupling reactions or nucleophilic substitution. Its bromine and thiocarbonyl groups allow for selective transformations, making it valuable in multi-step synthetic routes.

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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,210.00
inventory 1g
10-20 days ฿6,190.00
inventory 5g
10-20 days ฿12,290.00
inventory 25g
10-20 days ฿49,290.00

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2-Bromothiobenzamide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals and agrochemicals due to its reactivity in cyclization reactions. Commonly employed in the synthesis of thiazoles and benzothiazoles, which are key scaffolds in medicinal chemistry. Also utilized in the formation of bioactive molecules and functional materials through palladium-catalyzed coupling reactions or nucleophilic substitution. Its bromine and th

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals and agrochemicals due to its reactivity in cyclization reactions. Commonly employed in the synthesis of thiazoles and benzothiazoles, which are key scaffolds in medicinal chemistry. Also utilized in the formation of bioactive molecules and functional materials through palladium-catalyzed coupling reactions or nucleophilic substitution. Its bromine and thiocarbonyl groups allow for selective transformations, making it valuable in multi-step synthetic routes.

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