2-Acetyl-3-thiopheneboronic acid(contains varying amounts of Anhydride)

95%

Reagent Code: #137518
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CAS Number 36155-74-5

science Other reagents with same CAS 36155-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.99 g/mol
Formula C₆H₇BO₃S
badge Registry Numbers
MDL Number MFCD01318932
thermostat Physical Properties
Melting Point 120-130 °C
Boiling Point 393.9±52.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, argon-filled storage

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the production of thrombin inhibitors and other cardiovascular drugs. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, making it valuable in forming carbon-carbon bonds during the development of complex organic molecules. Commonly employed in research and development of active pharmaceutical ingredients (APIs) due to its reactivity with halogenated aromatics under palladium catalysis. Also utilized in the synthesis of heterocyclic compounds for medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,620.00
inventory 5g
10-20 days ฿24,160.00

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2-Acetyl-3-thiopheneboronic acid(contains varying amounts of Anhydride)
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Used as a key intermediate in pharmaceutical synthesis, particularly in the production of thrombin inhibitors and other cardiovascular drugs. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, making it valuable in forming carbon-carbon bonds during the development of complex organic molecules. Commonly employed in research and development of active pharmaceutical ingredients (APIs) due to its reactivity with halogenated aromatics under palladium catalysis. Also utilized in the
Used as a key intermediate in pharmaceutical synthesis, particularly in the production of thrombin inhibitors and other cardiovascular drugs. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, making it valuable in forming carbon-carbon bonds during the development of complex organic molecules. Commonly employed in research and development of active pharmaceutical ingredients (APIs) due to its reactivity with halogenated aromatics under palladium catalysis. Also utilized in the synthesis of heterocyclic compounds for medicinal chemistry applications.
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