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4-Chloro-2,6-dimethoxyphenylboronic acid is a specialized chemical compound with the molecular formula C9H10BClO4. It is characterized by the presence of a phenylboronic acid moiety, which is a functional group consisting of a boronic acid attached to a phenyl group. In this particular compound, it is further modified by chlorine and methoxy substituents. Boronic acids like 4-Chloro-2,6-dimethoxyphenylboronic acid play an important role in many areas of chemistry, including organic synthesis and material science, due to their unique ability to form reversible covalent complexes with sugars, amino acids, and other compounds.

1067228-90-3

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1067228-90-3 Usage

Uses

Used in Organic Synthesis:
4-Chloro-2,6-dimethoxyphenylboronic acid is used as a reagent in organic synthesis for its ability to form reversible covalent complexes with various compounds, such as sugars and amino acids. This property allows for the selective modification of organic molecules and the formation of new chemical bonds.
Used in Material Science:
In the field of material science, 4-Chloro-2,6-dimethoxyphenylboronic acid is utilized for its potential to create new materials with unique properties. The reversible covalent bonding capability of 4-CHLORO-2,6-DIMETHOXY PHENYLBORONIC ACID can be harnessed to develop materials with tailored characteristics, such as improved stability or specific interactions with other molecules.
Used in Suzuki Coupling Reactions:
4-Chloro-2,6-dimethoxyphenylboronic acid is used as a key component in Suzuki coupling reactions, a widely employed method for forming carbon-carbon bonds in the synthesis of complex organic molecules. This reaction is particularly valuable in the production of pharmaceuticals, agrochemicals, and advanced materials, where the formation of specific molecular structures is crucial for their function and performance.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Chloro-2,6-dimethoxyphenylboronic acid is utilized in the development of new drugs and drug candidates. Its unique chemical properties enable the synthesis of novel molecular structures with potential therapeutic effects. Additionally, its involvement in Suzuki coupling reactions can facilitate the creation of diverse and complex drug molecules, expanding the range of treatments available for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1067228-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,2,2 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1067228-90:
(9*1)+(8*0)+(7*6)+(6*7)+(5*2)+(4*2)+(3*8)+(2*9)+(1*0)=153
153 % 10 = 3
So 1067228-90-3 is a valid CAS Registry Number.

1067228-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Chloro-2,6-dimethoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names Boronic acid,B-(4-chloro-2,6-dimethoxyphenyl)

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:1067228-90-3 SDS

1067228-90-3Upstream product

1067228-90-3Relevant academic research and scientific papers

2-Arylpyrimidines: Novel CRF-1 receptor antagonists

Yoon, Taeyoung,De Lombaert, Stephane,Brodbeck, Robbin,Gulianello, Michael,Krause, James E.,Hutchison, Alan,Horvath, Raymond F.,Ge, Ping,Kehne, John,Hoffman, Diane,Chandrasekhar, Jayaraman,Doller, Dario,Hodgetts, Kevin J.

scheme or table, p. 4486 - 4490 (2009/04/08)

The design, synthesis and structure-activity relationship studies of a novel series of CRF-1 receptor antagonists, the 2-arylpyrimidines, are described. The effects of substitution on the aromatic ring and the pyrimidine core on CRF-1 receptor binding wer

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