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2,4-Imidazolidinedione, 3-ethyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55889-17-3

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55889-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55889-17-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55889-17:
(7*5)+(6*5)+(5*8)+(4*8)+(3*9)+(2*1)+(1*7)=173
173 % 10 = 3
So 55889-17-3 is a valid CAS Registry Number.

55889-17-3SDS

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 3-ethyl-1-phenyl-imidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Ethyl-1-phenyl-hydantoin

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:55889-17-3 SDS

55889-17-3Relevant academic research and scientific papers

Pyrimidines. Part 53. Novel Ring Transformation induced by the Substituent Effect of the Phenyl Group. Reaction of 5-Bromo-6-methyl-1-phenyluracil Derivates with Amines and Hydrazine to give Hydantoins and Pyrazolones

Hirota, Kosaku,Banno, Kazuo,Yamada, Yoshihiro,Senda, Shigeo

, p. 1137 - 1142 (2007/10/02)

Reaction of 5-bromo-6-methyluracil derivates (1), possessing a phenyl or para-substituted phenyl group at the 1-position of the uracil ring, with methylamine or hydrazine hydrate causes novel ring transformations to give 1-arylhydantoins (2) and 4-ureidop

Insecticidal phenyl hydantoin compounds

-

, (2008/06/13)

Novel phenyl hydantoin compounds are disclosed of the structure: STR1 wherein R1 and R2 are independently hydrogen, amino, nitro, halogen, hydroxy, substituted and unsubstituted lower alkyl, cycloalkyl, phenyl and lower alkenyl; and R3 is substituted and unsubstituted lower alkyl, lower alkenyl and cycloalkyl; as well as pesticidal methods employing said novel compounds; and pesticidal compositions containing said novel compounds.

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