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(3-Amino-5-nitrophenyl)boronic acid is a chemical compound with the molecular formula C6H6BNO4. It is a boronic acid derivative characterized by the presence of a boronic acid group, an amino group, and a nitro group attached to a phenyl ring. (3-AMINO-5-NITROPHENYL)BORONIC ACID is known for its applications in organic synthesis and medicinal chemistry, making it a valuable tool in the fields of chemistry and pharmaceutical research due to its unique chemical and structural properties.

89466-05-7

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89466-05-7 Usage

Uses

Used in Pharmaceutical Development:
(3-Amino-5-nitrophenyl)boronic acid is used as a key intermediate in the synthesis of pharmaceuticals for various therapeutic applications. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a versatile building block in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, (3-Amino-5-nitrophenyl)boronic acid serves as a reagent for the formation of complex organic molecules. Its boronic acid group facilitates the creation of new chemical bonds, which is crucial for the synthesis of a wide range of organic compounds.
Used as a Fluorescent Probe in Biochemistry:
(3-Amino-5-nitrophenyl)boronic acid has shown potential as a fluorescent probe for detecting and analyzing biomolecules. Its fluorescent properties allow researchers to track and visualize the behavior of biomolecules in biological systems, aiding in the study of biological processes and the development of diagnostic tools.
Used in Chemical Research:
As a compound with unique chemical and structural properties, (3-Amino-5-nitrophenyl)boronic acid is utilized in chemical research to explore new reaction mechanisms, investigate the properties of boronic acids, and develop novel synthetic methods. Its applications in research contribute to the advancement of chemical science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 89466-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,6 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89466-05:
(7*8)+(6*9)+(5*4)+(4*6)+(3*6)+(2*0)+(1*5)=177
177 % 10 = 7
So 89466-05-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7BN2O4/c8-5-1-4(7(10)11)2-6(3-5)9(12)13/h1-3,10-11H,8H2

89466-05-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H52651)  3-Amino-5-nitrobenzeneboronic acid, 97%   

  • 89466-05-7

  • 250mg

  • 1505.0CNY

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  • Alfa Aesar

  • (H52651)  3-Amino-5-nitrobenzeneboronic acid, 97%   

  • 89466-05-7

  • 1g

  • 4816.0CNY

  • Detail

89466-05-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-AMINO-5-NITROPHENYL)BORONIC ACID

1.2 Other means of identification

Product number -
Other names 3-dihydroxyboranyl-5-nitro-aniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89466-05-7 SDS

89466-05-7Relevant academic research and scientific papers

Indole and quinoline derivatives and its preparation method and application

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Paragraph 0192-0195, (2017/02/28)

The invention provides an indoloquinoline derivative, a preparation method and application thereof in preparing antitumor drugs and antiviral drugs. The chemical structure of the indoloquinoline derivative is shown as a formula I. Experiments show that a partly-boric-acid-modified indoloquinoline derivative and a non-boric-acid-modified indoloquinoline derivative have strong inhibition effect on various tumor cell strains, thereby being capable of being used for preparation of the antitumor drugs, and have strong antiviral activity, thereby being capable of being used for preparation of the antiviral drugs.

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