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73852-88-7

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73852-88-7 Usage

Uses

4-Iodophenylboronic acid, pinacol ester

Check Digit Verification of cas no

The CAS Registry Mumber 73852-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73852-88:
(7*7)+(6*3)+(5*8)+(4*5)+(3*2)+(2*8)+(1*8)=157
157 % 10 = 7
So 73852-88-7 is a valid CAS Registry Number.

73852-88-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
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  • Alfa Aesar

  • (H28190)  4-Iodobenzeneboronic acid pinacol ester, 97%   

  • 73852-88-7

  • 1g

  • 700.0CNY

  • Detail
  • Alfa Aesar

  • (H28190)  4-Iodobenzeneboronic acid pinacol ester, 97%   

  • 73852-88-7

  • 5g

  • 2150.0CNY

  • Detail
  • Aldrich

  • (699470)  4-Iodophenylboronicacidpinacolester  97%

  • 73852-88-7

  • 699470-1G

  • 634.14CNY

  • Detail
  • Aldrich

  • (699470)  4-Iodophenylboronicacidpinacolester  97%

  • 73852-88-7

  • 699470-5G

  • 1,882.53CNY

  • Detail

73852-88-7SDS

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-(4-iodophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 4-iodophenylboronic acid pinacol ester

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:73852-88-7 SDS

73852-88-7Relevant articles and documents

Fluorescent probe for detecting active oxygen molecule and preparation method and application thereof

-

Paragraph 0047-0051, (2021/10/27)

The invention discloses a fluorescent probe for detecting reactive oxygen molecules and a preparation method and application thereof, wherein the fluorescent probe comprises a quinolinium ion framework. The trimethylsilyl based on carbon-silicon single bo

Light- and Manganese-Initiated Borylation of Aryl Diazonium Salts: Mechanistic Insight on the Ultrafast Time-Scale Revealed by Time-Resolved Spectroscopic Analysis

Firth, James D.,Hammarback, L. Anders,Burden, Thomas J.,Eastwood, Jonathan B.,Donald, James R.,Horbaczewskyj, Chris S.,McRobie, Matthew T.,Tramaseur, Adam,Clark, Ian P.,Towrie, Michael,Robinson, Alan,Krieger, Jean-Philippe,Lynam, Jason M.,Fairlamb, Ian J. S.

supporting information, p. 3979 - 3985 (2021/02/03)

Manganese-mediated borylation of aryl/heteroaryl diazonium salts emerges as a general and versatile synthetic methodology for the synthesis of the corresponding boronate esters. The reaction proved an ideal testing ground for delineating the Mn species responsible for the photochemical reaction processes, that is, involving either Mn radical or Mn cationic species, which is dependent on the presence of a suitably strong oxidant. Our findings are important for a plethora of processes employing Mn-containing carbonyl species as initiators and/or catalysts, which have considerable potential in synthetic applications.

Generation of Organozinc Reagents from Arylsulfonium Salts Using a Nickel Catalyst and Zinc Dust

Yamada, Kodai,Yanagi, Tomoyuki,Yorimitsu, Hideki

, p. 9712 - 9718 (2021/01/09)

Readily available aryldimethylsulfonium triflates react with zinc powder under nickel catalysis via the selective cleavage of the sp2-hybridized carbon-sulfur bond to produce salt-free arylzinc triflates under mild conditions. This zincation displays superb chemoselectivity and thus represents a protocol that is complementary or orthogonal to existing methods. The generated arylzinc reagents show both high reactivity and chemoselectivity in palladium-catalyzed and copper-mediated cross-coupling reactions.

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