746177
MIBA
96%
Sinônimo(s):
5-Methoxy-2-iodophenylboronic acid
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1 G
R$ 742,00
About This Item
Fórmula empírica (Notação de Hill):
C7H8BIO3
Número CAS:
Peso molecular:
277.85
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.06
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Nível de qualidade
Ensaio
96%
Formulário
solid
características do produto alternativo mais ecológico
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
pf
202-207 °C
grupo funcional
iodo
categoria alternativa mais ecológica
, Aligned
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
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
chave InChI
XQYAEIDOJUNIGY-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
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.
Aplicação
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
Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect
Informações legais
This Product is licensed from GreenCentre Canada for non-commercial, research use only. Please contact GreenCentre Canada for information regarding commercial use of Product.
produto relacionado
Nº do produto
Descrição
Preços
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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The importance of amides as a component of biomolecules and synthetic products motivates the development of catalytic, direct amidation methods employing free carboxylic acids and amines that circumvent the need for stoichiometric activation or coupling reagents. ortho-Iodophenylboronic acid 4a has
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