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2,4-Imidazolidinedione, 5-[(2-chlorophenyl)methylene]-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88568-75-6

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88568-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88568-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,6 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88568-75:
(7*8)+(6*8)+(5*5)+(4*6)+(3*8)+(2*7)+(1*5)=196
196 % 10 = 6
So 88568-75-6 is a valid CAS Registry Number.

88568-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(2-chlorophenyl)methylidene]-3-methylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-Methyl-5-<o-chlor-benzyliden>-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:88568-75-6 SDS

88568-75-6Downstream Products

88568-75-6Relevant academic research and scientific papers

Synthesis of imidazol[1,5-a]indole-1,3-diones from imidazolidene-2,4-diones

Akeng'a,Read

, p. 11 - 16 (2008/09/16)

Copper and tributyltin hydride catalysed cyclization, through the N-aryl bond formation, of imidazolidine-2,4-diones (11-16,18) yielded imidazo[1,5-a]indole-1,3-diones (5-10) in high yields (72-100%). The ease of cyclization was found to be consistent with the normal halogen reactivity and the type of substituents. The highly substituted imidazole-2,4-dione 15 gave brominated 19 and tin incorporated heterocycles 20 when treated with copper bromide and tributyltin hydride, respectively.

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