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3-(3-methylphenyl)-1-[3-[4-[3-[(3-methylphenyl)carbamoylamino]propyl]piperazin-1-yl]propyl]urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55291-00-4

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55291-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55291-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,9 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55291-00:
(7*5)+(6*5)+(5*2)+(4*9)+(3*1)+(2*0)+(1*0)=114
114 % 10 = 4
So 55291-00-4 is a valid CAS Registry Number.

55291-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methylphenyl)-3-[3-[4-[3-[(3-methylphenyl)carbamoylamino]propyl]piperazin-1-yl]propyl]urea

1.2 Other means of identification

Product number -
Other names -

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:55291-00-4 SDS

55291-00-4Upstream product

55291-00-4Downstream Products

55291-00-4Relevant academic research and scientific papers

Anticonvulsant activity of N,N' bis[3 (3 substituted urea)propyl]piperazines

Chaturvedi,Barthwal,Parmar,Stenberg

, p. 454 - 456 (2007/10/09)

Several N,N' bis [3 (3 substituted urea)propyl]piperazines were synthesized and characterized by their sharp melting points, elemental analyses, and IR spectra. All substituted piperazines were found to possess anticonvulsant activity, which was reflected by 20-70% protection observed against pentylenetetrazole induced seizures in mice. Some of these compounds inhibited oxidation of pyruvic acid by rat brain homogenate. No correlation could be observed between the anticonvulsant activity possessed by these substituted piperazines and their ability to inhibit the oxidation of pyruvic acid.

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