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62134-54-7

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62134-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62134-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62134-54:
(7*6)+(6*2)+(5*1)+(4*3)+(3*4)+(2*5)+(1*4)=97
97 % 10 = 7
So 62134-54-7 is a valid CAS Registry Number.

62134-54-7SDS

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 4-(4-iodoanilino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names -

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:62134-54-7 SDS

62134-54-7Relevant academic research and scientific papers

Studies of hydrogen isotope scrambling during the dehalogenation of aromatic chloro-compounds with deuterium gas over palladium catalysts

Lockley, William J.S.,Venanzi, Niccolò A. E.,Crane, Georgie J.

, p. 531 - 552 (2020/09/22)

Catalytic dehalogenation of aromatic halides using isotopic hydrogen gas is an important strategy for labelling pharmaceuticals, biochemicals, environmental agents and so forth. To extend, improve and further understand this process, studies have been carried out on the scrambling of deuterium isotope with protium during the catalytic deuterodehalogenation of model aryl chlorides using deuterium gas and a palladium on carbon catalyst in tetrahydrofuran solution. The degree of scrambling was greatest with electron-rich chloroarene rings. The tetrahydrofuran solvent and the triethylamine base were not the source of the undesired protium; instead, it arose, substantially, from the water content of the catalyst, though other sources of protium may also be present on the catalyst. Replacement of the Pd/C catalyst with one prepared in situ by reduction of palladium trifluoroacetate with deuterium gas and dispersed upon micronised polytetrafluoroethylene led to much reduced scrambling (typically 0–6% compared with up to 40% for palladium on carbon) and to high atom% abundance, regiospecific labelling. The improved catalytic system now enables efficient polydeuteration via the dehalogenation of polyhalogenated precursors, making the procedure viable for the preparation of MS internal standards and, potentially, for high specific activity tritium labelling.

Synthesis of new ferrocene derivatives with rod-like structure

Okulov, Vladimir N.,Popov, Damir A.,Panfilova, Anastasia V.,Dyadchenko, Marina A.,Lemenovskii, Dmitrii A.,Dyadchenko, Victor P.

, p. 111 - 113 (2015/04/14)

The Suzuki-Miyaura cross-coupling of tris(4-ferrocenylphenyl)- and tris[4-(2-ferrocenylethynyl)phenyl]boroxines with functionalized iodoarenes gives new ferrocene derivatives of rod-like structure.

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