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4-Imidazolidinecarboxamide, 3-[4-(dimethylamino)phenyl]-4-methyl-2,5-dioxo-N,1-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83325-72-8

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83325-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83325-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,2 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83325-72:
(7*8)+(6*3)+(5*3)+(4*2)+(3*5)+(2*7)+(1*2)=128
128 % 10 = 8
So 83325-72-8 is a valid CAS Registry Number.

83325-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4'-N,N-dimethylaminophenyl)-3-phenyl-5-methyl-5-phenylamido-imidazolidin-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-(4-Dimethylamino-phenyl)-4-methyl-2,5-dioxo-1-phenyl-imidazolidine-4-carboxylic acid phenylamide

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:83325-72-8 SDS

83325-72-8Downstream Products

83325-72-8Relevant academic research and scientific papers

CONJUGATED SCHIFF'S BASES-14; CYCLOADDITION OF HETEROCUMULENES TO SOME 1-OXA-4-AZABUTADIENES

Moskal, Janusz,Moskal, Alexandra,Milart, Piotr

, p. 1787 - 1792 (2007/10/02)

1-Oxa-4-azabutadienes proved to be prone to react with some heterocumulenes after 1,3-cycloaddition patterns yielding various 5,5-disubstituted derivatives of 1,3-diaryl-hydanotoins as it was shown by the chemical and spectroscopic analysis.Relatively high yields, mild reaction conditions and a very weak effect of solvent polarity on the reaction rate suggested a synchroneous mechanism involving 1,2-migration of a substituent.

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