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N-Cyclohexyl 4-borono-2-chlorobenzamide is a chemical compound that is frequently utilized in scientific and medical research. It is particularly recognized for its role in click chemistry, a chemical reaction extensively used in biochemistry and materials science, owing to the presence of a boron atom in its structure. N-Cyclohexyl 4-borono-2-chlorobenzamide is characterized by a benzamide group, with a chlorine (Cl) atom on one of the carbon atoms, a boron (B) atom, and a cyclohexyl (C6H11) group attached to the nitrogen atom. As with many chemical substances, it requires careful handling due to potential hazards. While there is a significant amount of research in areas that use boron-containing molecules, specific information on N-Cyclohexyl 4-borono-2-chlorobenzamide, such as its toxicity, stability, or ecological effects, appears to be relatively scarce.

957034-65-0

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957034-65-0 Usage

Uses

Used in Scientific and Medical Research:
N-Cyclohexyl 4-borono-2-chlorobenzamide is used as a research compound for its application in click chemistry, a technique that is widely employed in the fields of biochemistry and materials science. The presence of the boron atom in its structure makes it a valuable tool for these research areas.
Used in Click Chemistry:
N-Cyclohexyl 4-borono-2-chlorobenzamide is used as a reactant in click chemistry reactions, which are known for their efficiency, specificity, and versatility in creating new chemical bonds. Its unique structure, including the boron atom, allows for the formation of stable and functional molecules that are useful in various applications.
Used in Biochemistry:
N-Cyclohexyl 4-borono-2-chlorobenzamide is used as a molecular building block in biochemistry, where it can be incorporated into more complex molecules or used to study the interactions between different biomolecules.
Used in Materials Science:
N-Cyclohexyl 4-borono-2-chlorobenzamide is used as a component in the development of new materials, particularly those that require the unique properties conferred by boron-containing compounds. Its use in materials science can lead to advancements in areas such as electronics, pharmaceuticals, and nanotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 957034-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,3 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 957034-65:
(8*9)+(7*5)+(6*7)+(5*0)+(4*3)+(3*4)+(2*6)+(1*5)=190
190 % 10 = 0
So 957034-65-0 is a valid CAS Registry Number.

957034-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names [3-chloro-4-(cyclohexylcarbamoyl)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:957034-65-0 SDS

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