Isoquinolin-7-yl-7-boronic acid

≥95%

Reagent Code: #90974
fingerprint
CAS Number 1092790-21-0

science Other reagents with same CAS 1092790-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.98 g/mol
Formula C₉H₈BNO₂
badge Registry Numbers
MDL Number MFCD08234617
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the formation of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the creation of carbon-carbon bonds, essential for constructing pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile tool in medicinal chemistry for developing new drugs. Additionally, it finds application in material science for designing advanced organic materials with specific electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,360.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Isoquinolin-7-yl-7-boronic acid
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in the formation of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the creation of carbon-carbon bonds, essential for constructing pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile tool in medicinal chemistry for developing new drugs. Additionally, it finds application in material scienc

Used primarily in organic synthesis, this compound serves as a key intermediate in the formation of complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the creation of carbon-carbon bonds, essential for constructing pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile tool in medicinal chemistry for developing new drugs. Additionally, it finds application in material science for designing advanced organic materials with specific electronic properties.

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...