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5-Benzyl-3-(benzyloxy)iMidazolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1248783-65-4

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1248783-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1248783-65-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,8,7,8 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1248783-65:
(9*1)+(8*2)+(7*4)+(6*8)+(5*7)+(4*8)+(3*3)+(2*6)+(1*5)=194
194 % 10 = 4
So 1248783-65-4 is a valid CAS Registry Number.

1248783-65-4SDS

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 5-benzyl-3-phenylmethoxyimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Benzyl-3-(benzyloxy)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:1248783-65-4 SDS

1248783-65-4Relevant academic research and scientific papers

Novel ureidoamides derived from amino acids: Synthesis and preliminary biological screening

Perkovic, Ivana,Butula, Ivan,Rajic, Zrinka,Hadjipavlou-Litina, Dimitra,Pontiki, Eleni,Zorc, Branka

, p. 151 - 161 (2011/05/02)

A series of novel amino acid ureidoamides 4a-o were prepared from N-(1-benzotriazolecarbonyl)-amino acid chloride 3, derived from L-alanine, L-valine, L-leucine, D-phenylglycine and L-phenylalanine, and the corresponding aminoalcohols (2-amino-1-ethanol, 3-amino-1-propanol and 5-amino-1-pentanol). The compounds were fully characterized by standard spectroscopic methods (IR, 1H and 13C NMR) and their structure was confirmed by elemental analysis. Antioxidant screenings (interaction with 1,1-diphenyl-2-picrylhydrazyl, soybean lipoxygenase inhibition activity, inhibition of linoleic acid lipid peroxidation) revealed that the prepared compounds possessed only modest activity. On the other hand, no significant antiproliferative activity against five human cell lines and very weak antimicrobial activity against several bacteria and fungi were detected.

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