2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetonitrile

96%

Reagent Code: #90653
fingerprint
CAS Number 138500-86-4

science Other reagents with same CAS 138500-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.12 g/mol
Formula C₁₄H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD02179459
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex molecules. Additionally, it is employed in the development of fluorescent dyes and sensors due to its ability to interact with specific analytes. The nitrile group further enhances its reactivity, allowing for transformations into amines, carboxylic acids, or heterocycles, broadening its utility in medicinal chemistry and material science.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 95.5-100
¹H NMR Spectrum Consistent with structure
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿830.00
inventory 5g
10-20 days ฿3,010.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetonitrile
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex molecules. Additionally, it is employed in the development of fluorescent dyes and sensors due to its ability to interact with specific analytes. The nitrile group further enhances its rea

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds essential for constructing complex molecules. Additionally, it is employed in the development of fluorescent dyes and sensors due to its ability to interact with specific analytes. The nitrile group further enhances its reactivity, allowing for transformations into amines, carboxylic acids, or heterocycles, broadening its utility in medicinal chemistry and material science.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...