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108847-76-3

108847-76-3

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108847-76-3 Usage

Uses

Reactant for:Pd2+ and Cu2+ catalyzed oxidative cross-couplingsPreparation of biologically and pharmacologically active moleculesSuzuki-Miyaura cross-coupling reactions

Check Digit Verification of cas no

The CAS Registry Mumber 108847-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,8,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108847-76:
(8*1)+(7*0)+(6*8)+(5*8)+(4*4)+(3*7)+(2*7)+(1*6)=153
153 % 10 = 3
So 108847-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H9BO2S2/c14-13(15)8-4-3-7-11-12(8)17-10-6-2-1-5-9(10)16-11/h1-7,14-15H

108847-76-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (L19833)  Thianthrene-1-boronic acid, tech. 90%   

  • 108847-76-3

  • 1g

  • 436.0CNY

  • Detail

  • Alfa Aesar

  • (L19833)  Thianthrene-1-boronic acid, tech. 90%   

  • 108847-76-3

  • 5g

  • 1478.0CNY

  • Detail

  • Aldrich

  • (512214)  1-Thianthrenylboronicacid  ≥95%

  • 108847-76-3

  • 512214-5G

  • 896.10CNY

  • Detail

108847-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Thianthrenylboronic acid

1.2 Other means of identification

Product number -
Other names Thianthren-1-ylboronic acid

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:108847-76-3 SDS

108847-76-3Downstream Products

108847-76-3Relevant articles and documents

Thianthrene-based oligomers as hole transporting materials

Swist, Agnieszka,Soloducho, Jadwiga,Data, Przemyslaw,Lapkowski, Mieczyslaw

, p. 193 - 209 (2013/09/24)

The thianthrene-arylene conjugated units have been designed and synthesized via Suzuki or Stille coupling reaction. The structures and properties of the synthesized compounds were characterized by 1HNMR, 13CNMR, MS, UV-Vis absorption

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