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652148-93-1

5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Pyridine,5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

    Cas No: 652148-93-1

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  • 652148-93-1 Structure

  • Basic information

    1. Product Name: 5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER
    2. Synonyms: 5-CHLOROPYRIDINE-2-BORONIC ACID PINACOLATE;5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER;3-CHLORO-6-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE;4-Bromo-2-methylpyrimidine;5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan -2-yl)pyridine;5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan
    3. CAS NO:652148-93-1
    4. Molecular Formula: C11H15BClNO2
    5. Molecular Weight: 239.51
    6. EINECS: N/A
    7. Product Categories: Pyridine;pyridine series
    8. Mol File: 652148-93-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.14
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER(652148-93-1)
    11. EPA Substance Registry System: 5-CHLOROPYRIDINE-2-BORONIC ACID PINACOL ESTER(652148-93-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 652148-93-1(Hazardous Substances Data)

652148-93-1 Usage

Uses

5-Chloropyridine-2-boronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 652148-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,1,4 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 652148-93:
(8*6)+(7*5)+(6*2)+(5*1)+(4*4)+(3*8)+(2*9)+(1*3)=161
161 % 10 = 1
So 652148-93-1 is a valid CAS Registry Number.

652148-93-1SDS

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 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 5-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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:652148-93-1 SDS

652148-93-1Relevant articles and documents

Nitrogen-containing heterocyclic derivative and organic electroluminescent device thereof

-

Paragraph 0154-0157; 0190-0192, (2021/11/26)

The invention provides a nitrogen-containing heterocyclic derivative and an organic electroluminescent device thereof, and belongs to the technical field of organic electroluminescence. The nitrogen-containing heterocyclic derivative has strong hole block

Synthesis of novel halopyridinylboronic acids and esters. Part 4: Halopyridin-2-yl-boronic acids and esters are stable, crystalline partners for classical Suzuki cross-coupling

Bouillon, Alexandre,Lancelot, Jean-Charles,Santos, Jana Sopkova De Oliveira,Collot, Valérie,Bovy, Philipppe R.,Rault, Sylvain

, p. 10043 - 10049 (2007/10/03)

This paper describes some methods for the synthesis and the isolation of novel 5 or 6-halopyridin-2-yl-boronic acids and esters 3, 4, 7. These compounds are prepared via a regioselective halogen-metal exchange using n-butyllithium and subsequent quenching with triisopropylborate starting from appropriate dihalopyridines. All substrates studied to date provided a single regioisomeric boronic acid or ester product. Additionally, these compounds have been found to undergo Pd-catalysed coupling with arylhalides and authorise a strategy to produce new pyridines libraries.

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