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2-(4-Ethyl-piperazin-1-yl)pyridine-5-boronic acid pinacol ester is a boronic acid derivative featuring a piperazine ring and a pyridine ring. It is widely recognized for its role in organic synthesis and medicinal chemistry, particularly as a reagent in Suzuki-Miyaura cross-coupling reactions, which are instrumental in forming carbon-carbon bonds. The presence of the pinacol ester group enhances the stability and solubility of the compound in organic solvents, facilitating its use in laboratory settings. This versatile chemical is a valuable asset in the development of new pharmaceuticals and advanced materials.

940285-00-7

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940285-00-7 Usage

Uses

Used in Organic Synthesis:
2-(4-Ethyl-piperazin-1-yl)pyridine-5-boronic acid pinacol ester is used as a reagent for Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds. Its application in this process is vital for creating complex organic molecules with potential applications in various fields.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2-(4-Ethyl-piperazin-1-yl)pyridine-5-boronic acid pinacol ester serves as a building block in the synthesis of biologically active molecules and pharmaceuticals. Its structural components contribute to the development of new drugs with improved therapeutic properties.
Used in Advanced Material Development:
2-(4-Ethyl-piperazin-1-yl)pyridine-5-boronic acid pinacol ester's versatility extends to the creation of advanced materials, where its unique chemical properties are harnessed to produce innovative products with specialized applications.

Check Digit Verification of cas no

The CAS Registry Mumber 940285-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,2,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 940285-00:
(8*9)+(7*4)+(6*0)+(5*2)+(4*8)+(3*5)+(2*0)+(1*0)=157
157 % 10 = 7
So 940285-00-7 is a valid CAS Registry Number.

940285-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-4-[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]piperazine

1.2 Other means of identification

Product number -
Other names -

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:940285-00-7 SDS

940285-00-7Downstream Products

940285-00-7Relevant academic research and scientific papers

Thiazolidine derivatives or salts thereof as an active ingredient an inhibitor Pim

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Paragraph 0665, (2018/10/19)

PROBLEM TO BE SOLVED: To provide compounds which have excellent Pim inhibitory action and are useful as pharmaceuticals.SOLUTION: A compound is a thiazolidine derivative represented by the general formula (1) in the figure, or a salt thereof. (In the formula, X represents O or S; Rrepresents a hydrogen atom or a Calkyl group; Z, Z, Z, Z, Zand Zeach independently represent CH or N; Y represents an optionally substituted, divalent Caromatic hydrocarbon group or the like; Am represents a disubstituted amino group, or an optionally substituted, nitrogen-containing saturated heterocyclic group; and Rand Reach independently represent a hydrogen atom, a halogen atom, an alkyl group or the like.)

IMIDAZOPYRIMIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER

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Paragraph 00270; 00278, (2018/04/12)

A compound of Formula (IA), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein A, R3, R4, R6, and R7 are as defined herein.

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