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4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl is a chemical compound characterized by the presence of a boronic acid, amide, and an aromatic ring in its structure. It features a piperidine ring, a common structural element in many pharmaceuticals, and is in its acid form due to the hydrochloride (HCl) component. The specific properties and applications of 4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl are largely dependent on the context of the scientific research it is utilized in, with boronic acids generally playing a role in pharmaceutical development and the synthesis of complex chemical structures.

957060-72-9

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957060-72-9 Usage

Uses

Used in Pharmaceutical Research:
4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl is used as a building block in the synthesis of pharmaceuticals for its ability to form stable complexes and participate in various chemical reactions. Its presence of a piperidine ring and boronic acid functionality makes it a versatile component in the development of new drugs.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl is used as a reagent for the formation of complex chemical structures. Its boronic acid group allows for reactions such as the Suzuki-Miyaura cross-coupling, which is crucial for creating new organic compounds with potential applications in various industries.
Used in Material Science:
4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl may also be utilized in material science as a component in the development of new materials with specific properties. 4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl's structural features could contribute to the creation of materials with tailored characteristics for use in various applications, such as sensors or advanced materials for electronics.
Used in Biochemical Research:
In biochemical research, 4-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid, HCl could be employed as a probe or modifier of biological systems. Its ability to form stable complexes and interact with biomolecules may allow it to be used in studying enzyme mechanisms, developing biosensors, or creating new bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 957060-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 957060-72:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*0)+(2*7)+(1*2)=189
189 % 10 = 9
So 957060-72-9 is a valid CAS Registry Number.

957060-72-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52650)  4-[2-(1-Piperidinyl)ethylcarbamoyl]benzeneboronic acid hydrochloride, 98%   

  • 957060-72-9

  • 250mg

  • 1029.0CNY

  • Detail
  • Alfa Aesar

  • (H52650)  4-[2-(1-Piperidinyl)ethylcarbamoyl]benzeneboronic acid hydrochloride, 98%   

  • 957060-72-9

  • 1g

  • 3293.0CNY

  • Detail

957060-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2-piperidin-1-ylethylcarbamoyl)phenyl]boronic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names OR3291

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:957060-72-9 SDS

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