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958244-59-2

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958244-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 958244-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,2,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 958244-59:
(8*9)+(7*5)+(6*8)+(5*2)+(4*4)+(3*4)+(2*5)+(1*9)=212
212 % 10 = 2
So 958244-59-2 is a valid CAS Registry Number.

958244-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-(2-iodophenoxy)benzene

1.2 Other means of identification

Product number -
Other names 2-bromo-2'-iododiphenyl ether

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:958244-59-2 SDS

958244-59-2Relevant articles and documents

A silicon-containing compound and comprising the silicon-containing compound of the organic electroluminescent device (by machine translation)

-

, (2019/04/15)

Provides improved emission efficiency silicon-containing compound and comprising the silicon-containing compound of the organic electroluminescent device. According to the present invention contemplates silicon-containing compound by the following formula 1 expressed. Type 1 . (by machine translation)

An efficient domino Sonogashira/double carbopalladation/C-H-activation reaction leading to fluorescent polycyclic aromatic hydrocarbons

Tietze, Lutz F.,Eichhorst, Christoph

, p. 919 - 927 (2015/05/27)

A facile synthesis of fluorescent polycyclic aromatic hydrocarbons through a highly productive palladium-catalyzed fourfold domino Sonogashira/double carbopalladation/C-H-activation process was developed.

Ambiphilic compounds: Synthesis and structure of a phosphane-borane with a flexible diphenyl ether tether

Bebbington, Magnus W. P.,Bouhadir, Ghenwa,Bourissou, Didier

, p. 4483 - 4486 (2008/02/12)

The preparation of desired phosphane-borane 1 involves selective lithiation trapping of 2-bromo-2′-iododiphenyl ether 3 to give bromophosphane 4 followed by a second lithiation/electrophilic trapping to install the boron fragment. The structure of the new

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