Welcome to LookChem.com Sign In|Join Free
  • or
2-(Piperidin-1-ylmethyl)phenylboronic acid, also known as PIPERONYL BORONIC ACID, is an organic compound characterized by the chemical formula C12H17BNO2. It is a derivative of boronic acid, featuring a piperidine ring and a phenyl group connected to the boronic acid functional group. 2-(Piperidin-1-ylmethyl)phenylboronic acid is recognized for its utility in various chemical and pharmaceutical applications due to its unique structural attributes.

878289-33-9

Post Buying Request

878289-33-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

878289-33-9 Usage

Uses

Used in Organic Synthesis:
2-(Piperidin-1-ylmethyl)phenylboronic acid is utilized as a building block in organic synthesis, particularly for the development of pharmaceuticals and other biologically active molecules. Its structural components make it a versatile intermediate for creating a range of complex organic compounds.
Used in Catalyst Preparation:
In the chemical industry, 2-(Piperidin-1-ylmethyl)phenylboronic acid is used as a component in the preparation of boronic acid-based catalysts. These catalysts are essential for accelerating various chemical reactions, enhancing the efficiency and selectivity of synthesis processes.
Used in Chemical Sensing and Molecular Recognition:
2-(Piperidin-1-ylmethyl)phenylboronic acid also finds application in the development of materials for chemical sensing and molecular recognition. Its unique functional group allows it to interact with specific molecules, making it useful in the design of sensors and recognition systems.
Used in Pharmaceutical Development:
2-(Piperidin-1-ylmethyl)phenylboronic acid has been investigated for its potential anti-tumor and anti-inflammatory properties. As a result, it is used in pharmaceutical research and development, where it may contribute to the creation of new drugs targeting cancer and inflammatory conditions.
Used in Research Applications:
In academic and research settings, 2-(Piperidin-1-ylmethyl)phenylboronic acid serves as a subject of study for understanding the properties and reactions of boronic acid derivatives, which can lead to advancements in synthetic methods and the discovery of new applications in medicine and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 878289-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,2,8 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 878289-33:
(8*8)+(7*7)+(6*8)+(5*2)+(4*8)+(3*9)+(2*3)+(1*3)=239
239 % 10 = 9
So 878289-33-9 is a valid CAS Registry Number.

878289-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(Piperidin-1-ylmethyl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 2-(Piperidin-1-ylmethyl)phenylboronic 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:878289-33-9 SDS

878289-33-9Downstream Products

878289-33-9Relevant academic research and scientific papers

Amination-reduction reaction as simple protocol for potential boronic molecular receptors. Insight in supramolecular structure directed by weak interactions

Adamczyk-Wo?niak, Agnieszka,Madura, Izabela,Pawe?ko, Alicja,Sporzyński, Andrzej,?ubrowska, Anna,?y?a, Jacek

, p. 199 - 205 (2011)

The synthesis of the potential molecular receptors in the amination-reduction reaction has been investigated within the model system comprising (2-formylphenyl)boronic acid and morpholine. The 3-amine substituted benzoxaborole was identified to be the intermediate of the synthesis and the unsubstituted benzoxaborole as the by-product resulting from reduction of the starting material. The insight into the reactivity of the starting materials as well as the intermediate benzoxaborole enabled significant rise in the yield of 2-(aminomethyl) phenylboronic acids synthesis. The solid state structure of 2-(piperidylmethyl)phenylboronic acid has been re-determined, and the description of the molecule and the crystal is given. The supramolecular layer structure directed by the weak C-H...O and C-H...π interactions was identified and scrutinized based on the geometry and Hirshfeld surface analyses. Versita Sp. z o.o.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 878289-33-9