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894787-96-3

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894787-96-3 Usage

Molecular Class

Pyrimidinone

Functionality

Selective, dual inhibitor of vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF) signaling pathways

Purpose

Potential anti-cancer and anti-angiogenesis agent

Applications

Treatment of hepatocellular carcinoma, metastatic colorectal cancer, and other solid tumor types

Mechanism of Action

Inhibits the growth of new blood vessels needed for tumor growth and spread

Research Status

Shown promising results in preclinical and clinical studies, currently being investigated for potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 894787-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,7,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 894787-96:
(8*8)+(7*9)+(6*4)+(5*7)+(4*8)+(3*7)+(2*9)+(1*6)=263
263 % 10 = 3
So 894787-96-3 is a valid CAS Registry Number.

894787-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-4-(4-fluorophenyl)-6-propan-2-yl-1H-pyrimidin-2-one

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:894787-96-3 SDS

894787-96-3Relevant articles and documents

Chemical Process

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Page/Page column 17, (2008/12/08)

A process for formation of a compound of formula (I) or a pharmaceutically acceptable salt thereof, (A chemical formula should be inserted here—please see paper copy enclosed herewith) I via a Heck reaction is described. Intermediates useful in the process and processes for making said intermediates are also described.

PROCESSES FOR THE MANUFACTURE OF ROSUVASTATIN AND INTERMEDIATES

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Page/Page column 6; 22-23, (2010/11/25)

A process for the manufacture of a compound of formula (V), useful for making rosuvastatin, by a stereoselective aldol reaction is described. Novel intermediates and processes to make them are also described.

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