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4-Nitrobenzeneboronic acid, 95%

Codice prodotto. 11312939
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11322939 5 g 5g
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Codice prodotto. 11312939 Fornitore Thermo Scientific Alfa Aesar N. del fornitore H27767.03
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CAS: 24067-17-2 | C6H6BNO4 | 166.93 g/mol

It is reagent used forligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings, ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines, Diels-Alder or C-H activation reactions, regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulations, N-arylation of phenylurea using copper acetylacetonate catalyst, environmentally benign one-pot synthesis through a double arylation process, copper-mediated cyanation, copper-catalyzed arylations regioselective glycosylations. Suzuki couplings followed by arylations, X-ray absorption on rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins. It is used in Preparation of combretastatin analogs as potential antitumor agents and human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is reagent used forligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings, ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines, Diels-Alder or C-H activation reactions, regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulations, N-arylation of phenylurea using copper acetylacetonate catalyst, environmentally benign one-pot synthesis through a double arylation process, copper-mediated cyanation, copper-catalyzed arylations regioselective glycosylations. Suzuki couplings followed by arylations, X-ray absorption on rhodium-grafted hydrotalcite catalyst for heterogeneous 1,4-addition reaction of organoboron reagents to electron deficient olefins. It is used in Preparation of combretastatin analogs as potential antitumor agents and human immunodeficiency virus (HIV) protease inhibitors with antiviral activities against drug-resistant viruses

Solubility
Slightly soluble in water.

Notes
Store in cool dry conditions. Incompatible with oxidizing agents.
TRUSTED_SUSTAINABILITY

Identificatori chimici

CAS 24067-17-2
Formula molecolare C6H6BNO4
Molecular Weight (g/mol) 166.93
Numero MDL MFCD00161360
InChI Key NSFJAFZHYOAMHL-UHFFFAOYSA-N
Sinonimo 4-nitrophenyl boronic acid, 4-nitrobenzeneboronic acid, p-nitrophenylboronic acid, 4-nitrophenylboronicacid, p-nitrophenyl boronic acid, 4-nitro phenyl boronic acid, boronic acid, 4-nitrophenyl, boronic acid, b-4-nitrophenyl, 4-borononitrobenzene
PubChem CID 2773552
IUPAC Name (4-nitrophenyl)boronic acid
SMILES OB(O)C1=CC=C(C=C1)[N+]([O-])=O

Specifica

Materiale o nome chimico 4-Nitrobenzeneboronic acid
Punto di fusione ∽285°C (decomposition)
Quantità 1 g
Informazioni di solubilità Slightly soluble in water.
Peso formulazione 166.93
Percent Purity 95%

RUO – Research Use Only

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