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3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID is a boronic acid compound with the chemical formula C11H14BClNO3. It is a derivative of phenylboronic acid, featuring a chlorine atom and an N-isopropylcarbamoyl group attached to the phenyl ring. 3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID is known for its unique reactivity and versatility in chemical reactions, making it a valuable component in various scientific and industrial applications.

850589-41-2

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850589-41-2 Usage

Uses

Used in Organic Synthesis:
3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID is used as a reagent in organic synthesis for its ability to participate in the Suzuki-Miyaura cross-coupling reaction. This reaction is a widely used method for forming carbon-carbon bonds, which is crucial for the creation of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID serves as a building block for the synthesis of various biologically active molecules. Its unique structure allows it to be a key component in the development of new pharmaceuticals, potentially leading to the discovery of novel treatments and therapies.
Used in Agrochemicals Synthesis:
3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID is also utilized in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals that can improve crop yields and protect plants from pests and diseases.
Used in Materials Science:
In the field of materials science, 3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID has potential applications due to its unique reactivity. It can be incorporated into the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Catalysis:
3-CHLORO-4-(N-ISOPROPYLCARBAMOYL)PHENYLBORONIC ACID's versatility in chemical reactions makes it a candidate for use in catalysis. It can potentially serve as a catalyst or be used in the development of new catalytic systems to enhance the efficiency and selectivity of various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 850589-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,8 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 850589-41:
(8*8)+(7*5)+(6*0)+(5*5)+(4*8)+(3*9)+(2*4)+(1*1)=192
192 % 10 = 2
So 850589-41-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13BClNO3/c1-6(2)13-10(14)8-4-3-7(11(15)16)5-9(8)12/h3-6,15-16H,1-2H3,(H,13,14)

850589-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-Chloro-4-(isopropylcarbamoyl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [3-chloro-4-(propan-2-ylcarbamoyl)phenyl]boronic 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:850589-41-2 SDS

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