Naphthalene-2-boronic Acid Pinacol Ester

≥97%

Reagent Code: #91221
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CAS Number 256652-04-7

science Other reagents with same CAS 256652-04-7

blur_circular Chemical Specifications

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Weight 254.13 g/mol
Formula C₁₆H₁₉O₂B
badge Registry Numbers
MDL Number MFCD05663868
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Naphthalene-2-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a key method for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a stable boronic ester reagent, facilitating the coupling of aryl or vinyl groups with halides or triflates. Its stability and ease of handling make it a preferred choice in complex molecular constructions. Additionally, it is utilized in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to introduce naphthalene moieties into conjugated systems. Its applications also extend to the synthesis of bioactive molecules and natural products, where precise control over molecular architecture is essential.

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Test Parameter Specification
Appearance White to Pale-yellow Powder or Crystals
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿410.00
inventory 25g
10-20 days ฿5,000.00

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Naphthalene-2-boronic Acid Pinacol Ester
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Naphthalene-2-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a key method for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a stable boronic ester reagent, facilitating the coupling of aryl or vinyl groups with halides or triflates. Its stability and ease of handling make it a preferred choice in complex molecular co

Naphthalene-2-boronic Acid Pinacol Ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is a key method for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a stable boronic ester reagent, facilitating the coupling of aryl or vinyl groups with halides or triflates. Its stability and ease of handling make it a preferred choice in complex molecular constructions. Additionally, it is utilized in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to introduce naphthalene moieties into conjugated systems. Its applications also extend to the synthesis of bioactive molecules and natural products, where precise control over molecular architecture is essential.

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