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Methanone, (4-hydroxy-3,5-diiodophenyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70036-74-7

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70036-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70036-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,3 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70036-74:
(7*7)+(6*0)+(5*0)+(4*3)+(3*6)+(2*7)+(1*4)=97
97 % 10 = 7
So 70036-74-7 is a valid CAS Registry Number.

70036-74-7Upstream product

70036-74-7Relevant articles and documents

Efficient and sustainable laccase-catalyzed iodination of: P -substituted phenols using KI as iodine source and aerial O2 as oxidant

Sdahl, Mark,Conrad, Jürgen,Braunberger, Christina,Beifuss, Uwe

, p. 19549 - 19559 (2019/07/05)

The laccase-catalyzed iodination of p-hydroxyarylcarbonyl- and p-hydroxyarylcarboxylic acid derivatives using KI as iodine source and aerial oxygen as the oxidant delivers the corresponding iodophenols in a highly efficient and sustainable manner with yields up to 93% on a preparative scale under mild reaction conditions.

Plasminogen activator inhibitor antagonists

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, (2008/06/13)

Compounds and pharmaceutical compositions useful as plasminogen activator inhibitor (PAI) antagonists are provided. In particular, methods of antagonizing PAI with substituted and unsubstituted aryl and heteroaryl ethers and thioethers, benzils, benzyl et

Highly chemoselective hydrogenolysis of iodoarenes

Faucher, Nicolas,Ambroise, Yves,Cintrat, Jean-Christophe,Doris, Eric,Pillon, Florence,Rousseau, Bernard

, p. 932 - 934 (2007/10/03)

The catalytic hydrodehalogenation reaction using molecular hydrogen and Pd/C has been revisited. It is shown that the speed of removal of halogen increases with increasing electronegativity I Br Cl. Nevertheless, selective dehydrohalogenation in compounds containing other reducible functions can be achieved only with iodine and not with bromine or chlorine. Selective deiodination of iodobenzophenone could be accomplished without reducing the carbonyl group. Hydrogenolysis of azidoiodoaromatic compounds to the corresponding azido compounds is high yielding. This selectivity was exploited for the labeling of benzophenone- and azido-containing compounds by deuterium and tritium.

Benzopenones useful in the treatment of insulin resistance and hyperglycemia

-

, (2008/06/13)

This invention provides compounds of Formula I having the structure STR1 wherein Y is STR2 R1 and R2 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, halogen, perfluoroalkyl of 1-6 carbon atoms, cycloalkyl of 3-8 carbon atoms, thienyl, furyl,

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