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N-(3-Chlorophenyl)-N'-(2-methoxyphenyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54964-90-8

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54964-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54964-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54964-90:
(7*5)+(6*4)+(5*9)+(4*6)+(3*4)+(2*9)+(1*0)=158
158 % 10 = 8
So 54964-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H13ClN2O2/c1-19-13-8-3-2-7-12(13)17-14(18)16-11-6-4-5-10(15)9-11/h2-9H,1H3,(H2,16,17,18)

54964-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-chlorophenyl)-3-(2-methoxyphenyl)urea

1.2 Other means of identification

Product number -
Other names N-(3-Chlorophenyl)-N'-(2-methoxyphenyl)urea

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:54964-90-8 SDS

54964-90-8Downstream Products

54964-90-8Relevant academic research and scientific papers

Unsymmetrically disubstituted urea derivatives: A potent class of antiglycating agents

Khan, Khalid M.,Saeed, Sumayya,Ali, Muhammad,Gohar, Madiha,Zahid, Javariya,Khan, Ambreen,Perveen, Shahnaz,Choudhary, M. Iqbal

experimental part, p. 2447 - 2451 (2009/09/05)

A series of unsymmetrically disubstituted urea derivatives 1-28 has been synthesized and screened for their antiglycation activity in vitro. Compounds 26 (IC50 = 4.26 ± 0.25 μM), 1 (IC50 = 5.8 ± 0.08 μM), 22 (IC50 = 4.26 ± 0.25 μM), 6 (IC50 = 6.4 ± 0.02 μM), 5 (IC50 = 6.6 ± 0.26 μM), 2 (IC50 = 7.02 ± 0.31 μM), 3 (IC50 = 7.14 ± 0.84 μM), 27 (IC50 = 7.27 ± 0.36 μM), 4 (IC50 = 8.16 ± 1.04 μM), 21 (IC50 = 8.4 ± 0.15 μM), 23 (IC50 = 9.0 ± 0.35 μM) and 13 (IC50 = 15.22 ± 6.7 μM) showed an excellent antiglycation activity far better than the standard (rutin, IC50 = 41.9 ± 2.3 μM). This study thus provides a series of potential molecules for further studies of antiglycation agents.

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