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918664-36-5

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918664-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918664-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,6,6 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 918664-36:
(8*9)+(7*1)+(6*8)+(5*6)+(4*6)+(3*4)+(2*3)+(1*6)=205
205 % 10 = 5
So 918664-36-5 is a valid CAS Registry Number.

918664-36-5SDS

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 4-(1-methyl-4,5-diphenylimidazol-2-yl)aniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-(1-methyl-4,5-diphenyl-1H-imidazol-2-yl)

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:918664-36-5 SDS

918664-36-5Relevant articles and documents

Synthesis of 2-substituted-N-[4-(1-methyl-4,5-diphenyl-1H-imidazole-2-yl) phenyl] acetamide derivatives and evaluation of theiranticancer activity

Oezkay, Yusuf,Isikdag, Ilhan,Incesu, Zerrin,Akalin, Guelsen

experimental part, p. 3320 - 3328 (2010/08/06)

In the present study 18 novel imidazole-(benz)azole and imidazoleepiperazine derivatives were synthesized in order to investigate their probable anticancer activity. The structures of the compounds were confirmed by IR,1H NMR and EI-MS spectral data. Cytotoxicity (MTT),analysis of DNA synthesis and detection of apoptotic DNA assays were applied to determine anticancer activity of the compounds against colon (HT-29) and breast (MCF-7) carcinoma cell lines. Most of the compounds,showed greater activity against HT-29 cells than MCF-7 cells. Some of them indicated considerable cytotoxicity against both of the carcinogenic cell lines. However,their inhibitory activity on DNA synthesis was relatively poor. Anticancer activity screening results revealed that 11,12 and 13 were the most active compounds in the series. They exhibited significant cytotoxicity against both of the carcinogenic cell lines and caused DNA fragmentation of the HT-29 cells.

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