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Benzene, 1,1'-oxybis[2-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102391-49-1

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102391-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102391-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,9 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102391-49:
(8*1)+(7*0)+(6*2)+(5*3)+(4*9)+(3*1)+(2*4)+(1*9)=91
91 % 10 = 1
So 102391-49-1 is a valid CAS Registry Number.

102391-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2′-oxybis(iodobenzene)

1.2 Other means of identification

Product number -
Other names Bis-(2-jod-phenyl)-aether

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:102391-49-1 SDS

102391-49-1Downstream Products

102391-49-1Relevant academic research and scientific papers

BIARYL HYDROXYTHIOPHENE GROUP IV TRANSITION METAL POLYMERIZATION CATALYSTS WITH CHAIN TRANSFER CAPABILITY

-

, (2022/02/05)

Catalyst systems that include a chain transfer agent and a metal-ligand complex according to formula (I).

Dibismuthanes in catalysis: From synthesis and characterization to redox behavior towards oxidative cleavage of 1,2-diols

Magre, Marc,Kuziola, Jennifer,N?thling, Nils,Cornella, Josep

supporting information, p. 4922 - 4929 (2021/06/16)

A family of aryl dinuclear bismuthane complexes has been successfully synthesized and characterized. The two bismuth centers are bonded to various xanthene-type backbones, which differ in ring-size and flexibility, resulting in complexes with different intramolecular Bi?Bi distances. Moreover, their pentavalent Bi(v) analogues have also been prepared and structurally characterized. Finally, the synergy between bismuth centers in catalysis has been studied by applying dinuclear bismuthanes5-8to the catalytic oxidative cleavage of 1,2-diols. Unfortunately, no synergistic effects were observed and the catalytic activities of dinuclear bismuthanes and triphenylbismuth are comparable.

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