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91493-19-5

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91493-19-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91493-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,9 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91493-19:
(7*9)+(6*1)+(5*4)+(4*9)+(3*3)+(2*1)+(1*9)=145
145 % 10 = 5
So 91493-19-5 is a valid CAS Registry Number.

91493-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1'-Biphenyl, 4-iodyl-

1.2 Other means of identification

Product number -
Other names 4-Phenyl-1-iodylbenzene

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:91493-19-5 SDS

91493-19-5Upstream product

91493-19-5Relevant articles and documents

IODOXYBENZENE A REMARKABLY CLOSE OZONE EQUIVALENT

Ranganathan, S.,Ranganathan, D.,Ramachandran, P. V.

, p. 3145 - 3152 (2007/10/02)

Iodoxybenzene is isoelectronic to ozone and several of its reactions proceed via pathways remarkably similar to that of ozone.An attractive feature of iodoxybenzene mediated reactions is the direct formation of products and the transformation of the reagent to iodobenzene.The formation of benzil and iodobenzene in good yields from diphenylacetylene provides support for the anticipated intermediate arising from ?4s+?2s addition.Iodoxybenzene transforms phenanthrene to phenanthrenequinone as a result of the initially formed 4+2 adduct undergoing C-H rupture, in preference to the C-C rupture.This change is parallel to the transformation of phenanthrene 9-carboxylic acid to phenanthrenequinone with ozone.The expected C-C rupture of the initially formed adduct does take place with acenaphthylene leading to naphthalic anhydride.The reaction of pyrene with iodoxybenzene leads to nearly equal amounts of the 4-5, 1-6 and 3-6 quinones involving attack on the bond of the lowest bond localisation energy and the atom of the lowest atom localization energy.This behaviour is similar to the action of ozone on benzopyrene.Iodoxybenzene transforms anthracene, just like ozone, to anthraquinone, in good yields.The involvement of transannular addition of iodoxybenzene, as is partly the case with ozone, is proved unlikely by reaction with 9, 10 dimethylanthracene which gave 10-methyl 9-anthraldehyde and 10-carboxy 9-anthraldehyde, involving the insertion of elements of iodoxybenzene to the aryl C-H bond.This tendency of iodoxybenzene has been further demonstrated by the following changes: diphenylmethane-->benzophenone; fluorene-->fluorenone and tetralin-->α-tetralone.Several of the transformations brought about with iodoxybenzene provide attractive synthetic routes, particularly to phenanthrenequinone, pyrenequinones and tetralone.Finally, just like the 2O3 --> 3O2 change, iodoxybenzene, and even more so, 4-iodoxybiphenyl, thermally fragment to iodobenzene and 4-iodobiphenyl.

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