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2-(Morpholino)phenylboronic acid is a chemical compound that belongs to the class of phenylboronic acids, characterized by the presence of a boronic acid functional group and a morpholine ring. It is a white solid with limited solubility in water and is widely used in organic synthesis and pharmaceuticals. Its ability to form stable complexes with diols and other Lewis bases has made it a promising candidate for applications in catalysis, drug discovery, and the development of fluorescence sensors and bioconjugates.

933052-52-9

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933052-52-9 Usage

Uses

Used in Organic Synthesis:
2-(Morpholino)phenylboronic acid is used as a reagent in organic chemical reactions for its ability to form stable complexes with diols and other Lewis bases, facilitating various synthetic transformations.
Used in Pharmaceutical Industry:
2-(Morpholino)phenylboronic acid is used as a building block in drug discovery due to its potential to interact with biological targets and modulate their activity, contributing to the development of new therapeutic agents.
Used in Catalysis:
2-(Morpholino)phenylboronic acid is employed as a catalyst or catalyst precursor in various chemical reactions, leveraging its ability to form stable complexes with Lewis bases to enhance reaction efficiency and selectivity.
Used in Fluorescence Sensors:
2-(Morpholino)phenylboronic acid is used as a component in the development of fluorescence sensors, capitalizing on its ability to form complexes with specific analytes, leading to changes in fluorescence properties for sensing applications.
Used in Bioconjugation:
2-(Morpholino)phenylboronic acid is utilized in the field of bioconjugation to attach biologically relevant molecules, such as peptides, proteins, or nucleic acids, to various surfaces or other molecules, enabling the creation of novel biofunctional materials and tools.
Used in Medical Research:
2-(Morpholino)phenylboronic acid has been investigated for its potential role in treating conditions such as diabetes and cancer, due to its ability to modulate biological processes and interact with specific targets, offering new avenues for therapeutic intervention.

Check Digit Verification of cas no

The CAS Registry Mumber 933052-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,0,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 933052-52:
(8*9)+(7*3)+(6*3)+(5*0)+(4*5)+(3*2)+(2*5)+(1*2)=149
149 % 10 = 9
So 933052-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BNO3/c13-11(14)9-3-1-2-4-10(9)12-5-7-15-8-6-12/h1-4,13-14H,5-8H2

933052-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-morpholin-4-ylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 2-Morpholinophenylboronic acid

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:933052-52-9 SDS

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