Methyl 4-bromo-3-hydroxythiophene-2-carboxylate

≥95%

Reagent Code: #47466
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CAS Number 95201-93-7

science Other reagents with same CAS 95201-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.07 g/mol
Formula C₆H₅BrO₃S
badge Registry Numbers
MDL Number MFCD00052081
thermostat Physical Properties
Melting Point 79-80°C
Boiling Point 247.9±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed away from light

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and a hydroxyl group, makes it a valuable precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecular frameworks. Additionally, it serves as a key building block in the synthesis of thiophene derivatives, which are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its ester functionality further allows for modifications, enabling the creation of diverse compounds with tailored properties for specific applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,507.00
inventory 100mg
10-20 days ฿585.00
inventory 250mg
10-20 days ฿1,197.00
inventory 1g
10-20 days ฿1,638.00

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Methyl 4-bromo-3-hydroxythiophene-2-carboxylate
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and a hydroxyl group, makes it a valuable precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecular frameworks. Additionally, it serves as a key building block in the synthesis of thiophene derivatives, which are often explored for their poten

This chemical is primarily utilized in organic synthesis as a versatile intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring both a bromo and a hydroxyl group, makes it a valuable precursor in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for constructing complex molecular frameworks. Additionally, it serves as a key building block in the synthesis of thiophene derivatives, which are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Its ester functionality further allows for modifications, enabling the creation of diverse compounds with tailored properties for specific applications.

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