4-(N,N-DiMethylaMino)Phenylboronic Acid Hydrochloride

98%

Reagent Code: #60918
label
Alias 4-Dimethylaminophenylboronic acid 4-Dimethylaminophenylboronic acid 4-(N,N-dimethylamino)phenylboronic acid 4-(N,N-dimethylamino)phenylboronic acid
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CAS Number 1150114-73-0

science Other reagents with same CAS 1150114-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.45832 g/mol
Formula C₈H₁₃BClNO₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds efficiently. It is also employed in the preparation of pharmaceutical intermediates and bioactive molecules due to its stability and reactivity. Additionally, it serves as a building block in the development of sensors and probes for detecting sugars and other analytes in biochemical research. Its boronic acid group enables it to interact with diols, making it useful in carbohydrate chemistry and glycobiology studies.

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Test Parameter Specification
Purity 98-100%
Melting Point 123-130
Appearance White to off-white powder

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,610.00
5g
10-20 days ฿7,200.00
200mg
10-20 days ฿590.00
4-(N,N-DiMethylaMino)Phenylboronic Acid Hydrochloride
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Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds efficiently. It is also employed in the preparation of pharmaceutical intermediates and bioactive molecules due to its stability and reactivity. Additionally, it serves as a building block in the development of sensors and probes for detecting sugars and other analytes in biochemical research. Its boronic acid group enables it to interact with diols, making it useful in carbohy

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to form carbon-carbon bonds efficiently. It is also employed in the preparation of pharmaceutical intermediates and bioactive molecules due to its stability and reactivity. Additionally, it serves as a building block in the development of sensors and probes for detecting sugars and other analytes in biochemical research. Its boronic acid group enables it to interact with diols, making it useful in carbohydrate chemistry and glycobiology studies.

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