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4-Nitrobenzeneboronic acid, 95%

CAS: 24067-17-2 | C6H6BNO4 | 166.93 g/mol

Supplier:  Thermo Scientific Chemicals H2776706

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Catalog No. AAH2776706

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Description

Description

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.
Specifications

Specifications

4-Nitrobenzeneboronic acid
∽285°C (decomposition)
MFCD00161360
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
NSFJAFZHYOAMHL-UHFFFAOYSA-N
(4-nitrophenyl)boronic acid
2773552
95%
24067-17-2
C6H6BNO4
5 g
Slightly soluble in water.
OB(O)C1=CC=C(C=C1)[N+]([O-])=O
166.93
166.93

Chemical Identifiers

24067-17-2
166.93
NSFJAFZHYOAMHL-UHFFFAOYSA-N
2773552
OB(O)C1=CC=C(C=C1)[N+]([O-])=O
C6H6BNO4
MFCD00161360
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
(4-nitrophenyl)boronic acid
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c

H302-H315-H319-H335

TSCA : No

Recommended Storage : Ambient temperatures

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