746177

MIBA

96%

• Sinónimos: 5-Methoxy-2-iodophenylboronic acid
• Fórmula empírica (notación de Hill): C₇H₈BIO₃
• Número de CAS: 89694-50-8
• Peso molecular: 277.85
• MDL number: MFCD26793796
• UNSPSC Code: 12352103
• PubChem Substance ID: 329765746
• NACRES: NA.06

Propiedades

• Quality Level: 100
• assay: 96%
• form: solid
• greener alternative product characteristics: Catalysis; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• mp: 202-207 °C
• functional group: iodo
• greener alternative category: , Aligned
• storage temp.: 2-8°C
• SMILES string: OB(O)C1=C(I)C=CC(OC)=C1
• InChI: 1S/C7H8BIO3/c1-12-5-2-3-7(9)6(4-5)8(10)11/h2-4,10-11H,1H3
• InChI key: XQYAEIDOJUNIGY-UHFFFAOYSA-N

Descripción

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalysis. Find details here.

Application

MIBA can be used to promote direct amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents.

Used to promote greener amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents.
Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect

Legal Information

This Product is licensed from GreenCentre Canada for non-commercial, research use only. Please contact GreenCentre Canada for information regarding commercial use of Product.

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable