(3-Chloro-5-hydroxyphenyl)boronic acid

≥95%

Reagent Code: #113210
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CAS Number 1214900-52-3

science Other reagents with same CAS 1214900-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.37 g/mol
Formula C₆H₆BClO₃
badge Registry Numbers
MDL Number MFCD15143456
thermostat Physical Properties
Boiling Point 403.9±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of drugs and bioactive molecules. Its boronic acid group enables efficient coupling with aryl halides, making it useful in creating complex organic structures. Additionally, it finds applications in the synthesis of materials for organic electronics, where precise molecular design is crucial. Its hydroxyl and chloro substituents further enhance its reactivity and versatility in tailored chemical transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,961.00
inventory 100mg
10-20 days ฿1,737.00
inventory 1g
10-20 days ฿8,091.00

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(3-Chloro-5-hydroxyphenyl)boronic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of drugs and bioactive molecules. Its boronic acid group enables efficient coupling with aryl halides, making it useful in creating complex organic structures. Additionally, it finds applications in the synthesis of materials for organic

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the development of drugs and bioactive molecules. Its boronic acid group enables efficient coupling with aryl halides, making it useful in creating complex organic structures. Additionally, it finds applications in the synthesis of materials for organic electronics, where precise molecular design is crucial. Its hydroxyl and chloro substituents further enhance its reactivity and versatility in tailored chemical transformations.

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