Welcome to LookChem.com Sign In|Join Free

CAS

  • or

615-42-9

Post Buying Request

615-42-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

615-42-9 Usage

Chemical Properties

clear yellow to brownish liquid

Uses

Different sources of media describe the Uses of 615-42-9 differently. You can refer to the following data:
1. suzuki reaction
2. 1,2-Diiodobenzene is useful for Suzuki reaction. It is also used in the synthesis of purino[8,9-f] phenanthridines. Further, it acts as a precursor for the synthesis of active pharmaceutical ingredients intermediate.

General Description

Photolysis of 1,2-diiodobenzene in cyclohexane, furan, benzene and benzene containing tetraphenylcyclopentadienone has been studied.

Check Digit Verification of cas no

The CAS Registry Mumber 615-42-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 615-42:
(5*6)+(4*1)+(3*5)+(2*4)+(1*2)=59
59 % 10 = 9
So 615-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H4I2/c7-5-3-1-2-4-6(5)8/h1-4H

615-42-9 Well-known Company Product Price

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

  • (B24425)  1,2-Diiodobenzene, 98%   

  • 615-42-9

  • 1g

  • 290.0CNY

  • Detail
  • Alfa Aesar

  • (B24425)  1,2-Diiodobenzene, 98%   

  • 615-42-9

  • 5g

  • 833.0CNY

  • Detail
  • Alfa Aesar

  • (B24425)  1,2-Diiodobenzene, 98%   

  • 615-42-9

  • 25g

  • 3673.0CNY

  • Detail

615-42-9SDS

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 1,2-Diiodobenzene

1.2 Other means of identification

Product number -
Other names 1,2-diiodo benzene

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:615-42-9 SDS

615-42-9Relevant articles and documents

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.

Direct Transformation of Arylamines to Aryl Halides via Sodium Nitrite and N-Halosuccinimide

Mukhopadhyay, Sushobhan,Batra, Sanjay

supporting information, p. 14622 - 14626 (2018/09/21)

A one-pot universal approach for transforming arylamines to aryl halides via reaction with sodium nitrite (NaNO2) and N-halosuccinimide (NXS) in DMF at room temperature under metal- and acid-free condition is described. This new protocol that is complementary to the Sandmeyer reaction, is suggested to involve the in situ generation of nitryl halide induce nitrosylation of aryl amine to form the diazo intermediate which is halogenated to furnish the aryl halide.

Aryne Insertion into I-I σ-Bonds

Rodriguez-Lojo, Diego,Cobas, Agustin,Pena, Diego,Perez, Dolores,Guitian, Enrique

supporting information; experimental part, p. 1363 - 1365 (2012/05/20)

A new protocol for the efficient synthesis of o-diiodoarenes has been developed. This method allows the synthesis of substituted and polycyclic o-diiodoarenes, which are difficult to obtain by classical methods. This diiodination process involves the formal insertion of arynes into the I-I σ-bond.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 615-42-9