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856-85-9

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856-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 856-85-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 856-85:
(5*8)+(4*5)+(3*6)+(2*8)+(1*5)=99
99 % 10 = 9
So 856-85-9 is a valid CAS Registry Number.

856-85-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(morpholinomethyl)-5,5-diphenylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3-morpholin-4-ylmethyl-5,5-diphenyl-imidazolidine-2,4-dione

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:856-85-9 SDS

856-85-9Relevant articles and documents

Microwave-assisted synthesis of some novel and potent antibacterial and antifungal compounds with biological screening

Bapna, Mayank,Parashar, Bharat,Sharma, Vinod K.,Chouhan, Lalit S.

, p. 1098 - 1106 (2012/08/07)

Hydantoins have widely been used as antiarrythmic, anticonvulsant and antitumor agents but recent research has shown a different and novel cytotoxic activity of hydantoins and its derivatives, i.e. anti HIV, antibacterial and antifungal. The following research article deals with the synthesis of hydantoins and their derivatives by Mannich reaction viz., 3-(substituted)-5,5- diphenylimidazolidine-2,4-dione and 1-(substituted)-3,5,5- triphenylimidazolidine-2,4-dione. The synthesised compounds are novel and some of the compounds showed good antibacterial and antifungal activity equivalent to the standards used. All synthetic procedures were carried out in a microwave and not by conventional methods, which led to speedy process and high yield for the same. Springer Science+Business Media, LLC 2011.

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