4-n-Pentylbenzeneboronic acid

97%

Reagent Code: #90583
label
Alias 4-pentylphenylboronic acid, 4-pentylphenylboronic acid, 4-pentylphenylboronic acid
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CAS Number 121219-12-3

science Other reagents with same CAS 121219-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.07 g/mol
Formula C₁₁H₁₇BO₂
badge Registry Numbers
MDL Number MFCD00995151
thermostat Physical Properties
Melting Point 82-84°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the development of drugs, particularly those targeting cancer and inflammation. Additionally, it is utilized in material science for the synthesis of organic electronic materials, such as polymers and small molecules for OLEDs and sensors. Its stability and reactivity make it a versatile reagent in research and industrial applications.

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Test Parameter Specification
Melting point 82-84
Purity (Neutralization Titration) 96.5-103.5%
Appearance Off-white powder
Infrared Spectrometry Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿230.00
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿530.00
inventory 25g
10-20 days ฿1,750.00
inventory 100g
10-20 days ฿5,450.00

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4-n-Pentylbenzeneboronic acid
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Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the development of drugs, particularly those targeting cancer and inflammation. Additionally, it is utilized in material science for the synthesis of

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the development of drugs, particularly those targeting cancer and inflammation. Additionally, it is utilized in material science for the synthesis of organic electronic materials, such as polymers and small molecules for OLEDs and sensors. Its stability and reactivity make it a versatile reagent in research and industrial applications.

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