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38257-52-2

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38257-52-2 Usage

General Description

N-(4-Iodophenyl)-N-phenylbenzenamine is a chemical compound consisting of a benzene ring substituted with a phenyl group and an iodine atom. It is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. N-(4-IODOPHENYL)-N-PHENYLBENZENAMINE is also known for its potential as a reagent in the development of new chemical reactions. N-(4-Iodophenyl)-N-phenylbenzenamine has potential applications in the field of medicinal chemistry and organic synthesis due to its unique structure and reactivity. It is important to handle this compound with caution and in accordance with proper safety protocols due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 38257-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,5 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38257-52:
(7*3)+(6*8)+(5*2)+(4*5)+(3*7)+(2*5)+(1*2)=132
132 % 10 = 2
So 38257-52-2 is a valid CAS Registry Number.

38257-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodo-N,N-diphenylaniline

1.2 Other means of identification

Product number -
Other names 4-Iodo-N,N-diphenyl-benzenamine

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:38257-52-2 SDS

38257-52-2Relevant articles and documents

A new route towards fluorescent organic nanoparticles with red-shifted emission and increased colloidal stability

Amro, Kassem,Daniel, Jonathan,Clermont, Guillaume,Bsaibess, Talia,Pucheault, Mathieu,Genin, Emilie,Vaultier, Michel,Blanchard-Desce, Mireille

, p. 1903 - 1909 (2014)

Suzuki-Miyaura cross-coupling reaction with a new boron reagent has been used to conveniently and efficiently synthetize a dipolar chromophore having an elongated π-conjugated system (i.e., bithiophene based), which displays a red-shifted emission while m

ORGANIC LIGHT-EMITTING DIODE MATERIALS

-

Paragraph 0546, (2018/08/09)

Described herin are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moeity D, each moiety D is covalently attached to either the moeity B or the moeity A, and each B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D and B are defined herein.

Rapid Iododeboronation with and without Gold Catalysis: Application to Radiolabelling of Arenes

Webster, Stacey,O'Rourke, Kerry M.,Fletcher, Conor,Pimlott, Sally L.,Sutherland, Andrew,Lee, Ai-Lan

supporting information, p. 937 - 943 (2017/12/26)

Radiopharmaceuticals that incorporate radioactive iodine in combination with single-photon emission computed tomography imaging play a key role in nuclear medicine, with applications in drug development and disease diagnosis. Despite this importance, there are relatively few general methods for the incorporation of radioiodine into small molecules. This work reports a rapid air- and moisture-stable ipso-iododeboronation procedure that uses NIS in the non-toxic, green solvent dimethyl carbonate. The fast reaction and mild conditions of the gold-catalysed method led to the development of a highly efficient process for the radiolabelling of arenes, which constitutes the first example of an application of homogenous gold catalysis to selective radiosynthesis. This was exemplified by the efficient synthesis of radiolabelled meta-[125I]iodobenzylguanidine, a radiopharmaceutical that is used for the imaging and therapy of human norepinephrine transporter-expressing tumours.

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