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Benzenamine, 4-[(5-chloro-2-pyrimidinyl)oxy]-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111986-56-2

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111986-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111986-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,9,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111986-56:
(8*1)+(7*1)+(6*1)+(5*9)+(4*8)+(3*6)+(2*5)+(1*6)=132
132 % 10 = 2
So 111986-56-2 is a valid CAS Registry Number.

111986-56-2SDS

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-(5-chloropyrimidin-2-yl)oxy-3-methylaniline

1.2 Other means of identification

Product number -
Other names 4-(5-chloro-2-pyrimidinyloxy)-3-methylaniline

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:111986-56-2 SDS

111986-56-2Relevant academic research and scientific papers

hTERT MODULATORS AND METHODS OF USE

-

Paragraph 0093; 0094; 0095; 0117, (2018/02/28)

The present invention provides hTERT modulators and methods for producing and using the same. In particular, the present invention provide a compound of the formula as described herein. Some aspects of the invention are based on the characterization of the effect of hTERT core promoter region mutants on the 5-12 G-quadruplex structure and its stability. It is believed that some of the compounds of the invention bind selectively to the G-quadruplex in the hTERT core promoter mutant, which results in reversal of the effect of mutant promoter activation.

Synthesis and antitumor activities of novel benzoylphenylurea derivatives

Okada,Koyanagi,Yamada,Haga

, p. 2308 - 2315 (2007/10/02)

Seventy novel benzoylphenylurea compounds were synthesized and their antitumor activities were examined in vivo against P388 leukemia. N-(2-Nitrobenzoyl)-N'-[4-(2-pyrimidinyloxy)phenyl]ureas showed the highest antitumor activities when dosed intraperitoneally or orally. Their structure-activity relationships were examined with particular focus on the position and the variety of substituent on each aryl ring.

N-benzoyl urea compounds, antitumorous compositions containing them

-

, (2008/06/13)

An N-benzoyl urea compound having the formula: STR1 wherein X is a hydrogen atom, a halogen atom or a nitro group, n is an integer of from 1 to 3, and Q is STR2 wherein Y1 is an unsubstituted or substituted alkyl group, or an alkoxy or alkoxyca

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