Login   |   Create New Account sales@aaronchem.com

Home > Products> 493035-82-8
493035-82-8

(4-Hydroxy-2-methyl)phenylboronic acid

Catalog#: AR00DEO1  |   CAS#: 493035-82-8  |   MDL#: MFCD03788424  |   MF: C7H9BO3  |   MW: 151.9556

Packsize Purity Price Availability Quantity
250mg 98% $9.00 Global Stock Buy Now Add To Cart
1g 98% $26.00 Global Stock Buy Now Add To Cart
5g 98% $123.00 Global Stock Buy Now Add To Cart
25g 98% $498.00 Global Stock Buy Now Add To Cart
  • Description
  • Application
  • Related Products
  • Featured Products
  • Safety Information
Catalog Number AR00DEO1
Chemical Name (4-Hydroxy-2-methyl)phenylboronic acid
CAS Number 493035-82-8
Molecular Formula C7H9BO3
Molecular Weight 151.9556
MDL Number MFCD03788424
SMILES Oc1ccc(c(c1)C)B(O)O

4-Hydroxy-2-methylphenylboronic acid, also known as $name$, is a valuable molecule widely used in chemical synthesis processes. As a versatile boronic acid derivative, it serves as a crucial component in the formation of various carbon-carbon and carbon-heteroatom bonds in organic reactions.$name$ is particularly prized for its role in Suzuki-Miyaura cross-coupling reactions, a fundamental tool in modern organic synthesis. In this reaction, $name$ acts as a boron source, enabling the coupling of an aryl or vinyl halide with an organic boronic acid to form a new carbon-carbon bond. This method has revolutionized the construction of complex organic molecules, making $name$ an indispensable building block for the synthesis of pharmaceuticals, agrochemicals, and materials.Furthermore, $name$ can participate in other important reactions such as Chan-Lam coupling, Borylation, and Sonogashira coupling, expanding its utility in the synthesis of a wide range of organic compounds. Its ability to undergo diverse transformations underscores its significance in the development of new chemical entities and functional materials.In summary, $name$ plays a crucial role in modern organic synthesis as a key reagent for the construction of complex molecules through various cross-coupling reactions. Its versatility and compatibility with different reaction conditions make it a valuable asset for chemists seeking to streamline and diversify their synthetic strategies.
29274-28-0

1H-Pyrazolo[3,4-b]pyridine, 4-chloro-

29274-28-0

$4.00/100mg, $5.00/250mg, $12.00/1g, $45.00/5g, $87.00/10g, $208.00/25g, $693.00/100g,

118994-90-4

Oxazole-5-carboxylic acid

118994-90-4

$4.00/250mg, $6.00/1g, $27.00/5g, $51.00/10g, $112.00/25g, $446.00/100g,

885588-14-7

METHYL 2-BROMO-5-FLUOROISONICOTINATE

885588-14-7

$5.00/100mg, $7.00/250mg, $12.00/1g, $39.00/5g, $77.00/10g, $181.00/25g, $664.00/100g,

771510-32-8

5,7-Dichloro-3-isopropylpyrazolo[1,5-a]pyrimidine

771510-32-8

$18.00/250mg, $52.00/1g, $243.00/5g, $416.00/10g, $831.00/25g, $1,385.00/50g,

2300174-87-0

(2R,4R)-4-Fluoro-2-methylpyrrolidineHCl

2300174-87-0

$175.00/100mg, $279.00/250mg, $726.00/1g,

2259853-06-8

2,6-Dibenzyloxy-3-iodopyridine

2259853-06-8

$9.00/100mg, $18.00/250mg, $44.00/1g, $137.00/5g, $521.00/25g, $1,303.00/100g,

GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

Home| Products| Terms & Conditions| Ordering & Shipping| Company| Contact us

© 2019 Aaron Chemicals LLC. All Rights Reserved.