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1073353-78-2

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1073353-78-2 Usage

Uses

2,3-Dichloropyridine-4-boronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 1073353-78-2 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, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1073353-78:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*5)+(3*3)+(2*7)+(1*8)=142
142 % 10 = 2
So 1073353-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14BCl2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-6-15-9(14)8(7)13/h5-6H,1-4H3

1073353-78-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H27498)  2,3-Dichloropyridine-4-boronic acid pinacol ester, 95%   

  • 1073353-78-2

  • 250mg

  • 1049.0CNY

  • Detail
  • Alfa Aesar

  • (H27498)  2,3-Dichloropyridine-4-boronic acid pinacol ester, 95%   

  • 1073353-78-2

  • 1g

  • 2421.0CNY

  • Detail
  • Aldrich

  • (710105)  2,3-Dichloropyridine-4-boronicacidpinacolester  97%

  • 1073353-78-2

  • 710105-1G

  • 954.72CNY

  • Detail

1073353-78-2SDS

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

1.2 Other means of identification

Product number -
Other names 2,3-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:1073353-78-2 SDS

1073353-78-2Downstream Products

1073353-78-2Relevant articles and documents

Asymmetric synthesis of 1-heteroaryl-1-arylalkyl tertiary alcohols and 1-pyridyl-1-arylethanes by lithiation-borylation methodology

Watson, Charlotte G.,Aggarwal, Varinder K.

supporting information, p. 1346 - 1349 (2013/05/09)

The synthesis of highly enantioenriched α-heterocyclic tertiary alcohols has been achieved via lithiation-borylation of a configurationally stable lithiated carbamate and heterocyclic pinacol boronic esters followed by oxidation. Protodeboronation of the α-heterocyclic tertiary boronic esters using TBAF·3H2O or CsF gave highly enantioenriched 1-pyridyl-1-arylethanes in high er.

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