5-Bromothiophene-2-carbonyl Chloride

98%

Reagent Code: #149640
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CAS Number 31555-60-9

science Other reagents with same CAS 31555-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.5 g/mol
Formula C₆H₂BrClOS
badge Registry Numbers
MDL Number MFCD03421417
thermostat Physical Properties
Melting Point 36-38 °C(lit.)
Boiling Point 126 °C at 14 Torr (lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its reactivity allows for the introduction of the 5-bromothiophene moiety into larger molecules, making it valuable in the production of organic semiconductors and conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and solar cells. Also employed in the preparation of dyes, fluorescent probes, and functional materials where bromine serves as a handle for further cross-coupling reactions like Suzuki or Stille couplings.

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Test Parameter Specification
Appearance solid or liquid
Purity 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿4,466.00

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5-Bromothiophene-2-carbonyl Chloride
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its reactivity allows for the introduction of the 5-bromothiophene moiety into larger molecules, making it valuable in the production of organic semiconductors and conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and solar cells. Also employed in the preparation of dyes, fluorescent probes, and functional materials

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its reactivity allows for the introduction of the 5-bromothiophene moiety into larger molecules, making it valuable in the production of organic semiconductors and conjugated polymers for electronic devices such as organic field-effect transistors (OFETs) and solar cells. Also employed in the preparation of dyes, fluorescent probes, and functional materials where bromine serves as a handle for further cross-coupling reactions like Suzuki or Stille couplings.

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