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827031-01-6

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827031-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 827031-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,7,0,3 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 827031-01:
(8*8)+(7*2)+(6*7)+(5*0)+(4*3)+(3*1)+(2*0)+(1*1)=136
136 % 10 = 6
So 827031-01-6 is a valid CAS Registry Number.

827031-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-(4-phenoxyphenyl)quinazolin-4-amine

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:827031-01-6 SDS

827031-01-6Relevant articles and documents

Discovery of 2-chloro-N-(4-methoxyphenyl)-N-methylquinazolin-4-amine (EP128265, MPI-0441138) as a potent inducer of apoptosis with high in vivo activity

Sirisoma, Nilantha,Kasibhatla, Shailaja,Pervin, Azra,Zhang, Hong,Jiang, Songchun,Willardsen, J. Adam,Anderson, Mark B.,Baichwal, Vijay,Mather, Gary G.,Jessing, Kevin,Hussain, Raouf,Hoang, Khanh,Pleiman, Christopher M.,Tseng, Ben,Drewe, John,Sui, Xiong Cai

, p. 4771 - 4779 (2008)

Using a live cell, high-throughput caspase-3 activator assay, we have identified a novel series of 4-anilinoquinazolines as inducers of apoptosis. In this report, we discuss the discovery of 2-chloro-N-(4-methoxyphenyl)-N- methylquinazolin-4-amine, compound 2b (EP128265, MPI-0441138) as a highly active inducer of apoptosis (EC50 for caspase activation of 2 nM) and as a potent inhibitor of cell proliferation (GI50 of 2 nM) in T47D cells. Compound 2b inhibited tubulin polymerization, was effective in cells overexpressing ABC transporter Pgp-1, and was efficacious in the MX-1 human breast and PC-3 prostate cancer mouse models. In contrast to the SAR of 4-anilinoquinazolines as EGFR kinase inhibitors, the methyl group on the nitrogen linker was essential for the apoptosis-inducing activity of 4-anilinoquinazolines and substitution in the 6- and 7-positions of the quinazoline core structure decreased potency.

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