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1073353-98-6

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1073353-98-6 Usage

Uses

2,5-Dichloropyridine-4-boronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 1073353-98-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,5 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1073353-98:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*5)+(3*3)+(2*9)+(1*8)=146
146 % 10 = 6
So 1073353-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-9(14)15-6-8(7)13/h5-6H,1-4H3

1073353-98-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H27699)  2,5-Dichloropyridine-4-boronic acid pinacol ester, 95%   

  • 1073353-98-6

  • 250mg

  • 1107.0CNY

  • Detail
  • Alfa Aesar

  • (H27699)  2,5-Dichloropyridine-4-boronic acid pinacol ester, 95%   

  • 1073353-98-6

  • 1g

  • 2548.0CNY

  • Detail

1073353-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 2,5-dichloro-4-(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:1073353-98-6 SDS

1073353-98-6Downstream Products

1073353-98-6Relevant articles and documents

Understanding the Activation of Air-Stable Ir(COD)(Phen)Cl Precatalyst for C-H Borylation of Aromatics and Heteroaromatics

Slack, Eric D.,Colacot, Thomas J.

supporting information, p. 1561 - 1565 (2021/02/20)

A newly developed robust catalyst [Ir(COD)(Phen)Cl] (A) was used for the C-H borylation of three dozen aromatics and heteroaromatics with excellent yield and selectivity. Activation of the catalyst was identified by the use of catalytic amounts of water, alcohols, etc., when B2pin2 was used in noncoordinating solvents, while for THF catalytic use of HBpin was required. The results were on par with the in situ based expensive system [Ir(OMe)(COD)]2/dtbbpy or Me4Phen.

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