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3-(ETHOXYCARBONYL)PYRIDINE-5-BORONIC ACID PINACOL ESTER is a chemical compound that features a boronic acid and a pyridine ring. It is recognized for its capacity to form stable complexes with a range of organic molecules, which makes it a valuable asset in the development of innovative pharmaceuticals and agrochemicals. The pinacol ester group in its structure contributes to its stability and solubility in organic solvents, facilitating its use in laboratory settings. 3-(ETHOXYCARBONYL)PYRIDINE-5-BORONIC ACID PINACOL ESTER is a versatile and significant chemical building block with a broad spectrum of potential applications in organic chemistry.

916326-10-8

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  • Featured products ethyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)nicotinate

    Cas No: 916326-10-8

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916326-10-8 Usage

Uses

Used in Pharmaceutical Industry:
3-(ETHOXYCARBONYL)PYRIDINE-5-BORONIC ACID PINACOL ESTER is used as a key intermediate in the synthesis of various pharmaceutical compounds for its ability to form stable complexes with organic molecules, aiding in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 3-(ETHOXYCARBONYL)PYRIDINE-5-BORONIC ACID PINACOL ESTER is utilized as a building block in the creation of crop protection products, leveraging its complex-forming properties to enhance the effectiveness of these products.
Used in Organic Synthesis:
3-(ETHOXYCARBONYL)PYRIDINE-5-BORONIC ACID PINACOL ESTER is employed as a versatile reagent in organic synthesis for its stability and solubility, making it easier to handle and manipulate in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 916326-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,3,2 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 916326-10:
(8*9)+(7*1)+(6*6)+(5*3)+(4*2)+(3*6)+(2*1)+(1*0)=158
158 % 10 = 8
So 916326-10-8 is a valid CAS Registry Number.
InChI:InChI=1S/C14H20BNO4/c1-6-18-12(17)10-7-11(9-16-8-10)15-19-13(2,3)14(4,5)20-15/h7-9H,6H2,1-5H3

916326-10-8SDS

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 3-(Ethoxycarbonyl)pyridine-5-boronic acid pinacol ester

1.2 Other means of identification

Product number -
Other names ETHYL NICOTINATE-5-PINACOLBORONATE

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:916326-10-8 SDS

916326-10-8Relevant articles and documents

Synthesis of ethyl nicotinate-5-boronic acid pinacol ester and its application toward Suzuki coupling

Leblanc, Yves,Cerat, Pascal

, p. 2775 - 2781 (2008)

A method for the synthesis and isolation of pure ethyl nicotinate-5-boronic acid pinacol ester has been described. This boronate ester was used to prepare C2-C5 heteroarylnicotinates in good yields. Copyright Taylor & Francis Group, LLC.

PHTHALAZINES AS POTASSIUM ION CHANNEL INHIBITORS

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Page/Page column 58, (2014/09/29)

A compound of formula (I), wherein A, R1, R3, and R24 are described herein. The compounds are useful as inhibitors of potassium channel function and in the treatment and prevention of arrhythmia, IKur-associated disorders, and other disorders mediated by ion channel function.

PYRROLOPYRIDAZINES AS POTASSIUM ION CHANNEL INHIBITORS

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Page/Page column 49, (2014/09/29)

A compound of formula (I) wherein A, R1, R3, and R24 are described herein. The compounds are useful as inhibitors of potassium channel function and in the treatment of arrhythmia, IKur-associated disorders, and other disorders mediated by ion channel function.

Regioselective conversion of arenes to N-aryl-1,2,3-triazoles Using C-H Borylation

Srinivasan, Rajavel,Coyne, Anthony G.,Abell, Chris

supporting information, p. 11680 - 11684 (2014/10/15)

A one-pot protocol for the synthesis of N-aryl 1,2,3-triazoles from arenes by an iridium-catalyzed C-H borylation/copper catalyzed azidation/click sequence is described. 1mol % of Cu(OTf)2 was found to efficiently catalyze both the azidation and the click reaction. The applicability of this method is demonstrated by the late-stage chemoselective installation of 1,2,3-triazole moiety into unactivated molecules of pharmaceutical importance.

PYRROLOTRIAZINES AS POTASSIUM ION CHANNEL INHIBITORS

-

Page/Page column, (2014/09/29)

A compound of formula (I) wherein A, R1, R3, and R24 are described herein. The compounds are useful as inhibitors of potassium channel function and in the treatment of arrhythmia, maintaining normal sinus rhythm, IKur-associated disorders, and other disorders mediated by ion channel function.

PI3 KINASE/mTOR DUAL INHIBITOR

-

Page/Page column 5, (2012/07/28)

The present invention provides an imidazo[4,5-c]quinolin-2-one compound, or a pharmaceutically acceptable salt thereof, that inhibits both PI3K and mTOR and, therefore, is useful in the treatment of cancer.

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