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849217-50-1

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849217-50-1 Usage

Chemical structure

The compound has a cyclopropane ring and a carboxamide group, with fluorine, hydroxy, methoxy, quinolinyl, and phenyl groups attached to it.

Potential pharmaceutical or biological activity

The presence of various functional groups suggests that the compound may have potential pharmaceutical or biological activity.

Structural features

The compound has structural features that are often found in bioactive molecules, which may contribute to its potential pharmaceutical or biological activity.

Further experimentation and analysis required

Further experimentation and analysis are needed to determine the specific properties and potential uses of this chemical.

Fluorine atoms

The compound contains two fluorine atoms, which may contribute to its reactivity and stability.

Hydroxy and methoxy groups

The presence of hydroxy and methoxy groups may affect the compound's solubility and reactivity.

Quinolinyl group

The quinolinyl group is a common structural feature in many bioactive molecules and may contribute to the compound's potential biological activity.

Phenyl groups

The presence of phenyl groups may affect the compound's lipophilicity and stability.

Carboxamide group

The carboxamide group may contribute to the compound's hydrogen bonding capacity and solubility in water.

Complex compound

The compound is a complex molecule with multiple functional groups, which may contribute to its potential pharmaceutical or biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 849217-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,2,1 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 849217-50:
(8*8)+(7*4)+(6*9)+(5*2)+(4*1)+(3*7)+(2*5)+(1*0)=191
191 % 10 = 1
So 849217-50-1 is a valid CAS Registry Number.

849217-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N1'-[3-fluoro-4-[(7-hydroxy-6-methoxy-4-quinolyl)oxy]phenyl]-N1-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide

1.2 Other means of identification

Product number -
Other names N'-(3-fluoro-4-(7-hydroxy-6-methoxyquinolin-4-yloxy)phenyl)-N-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide

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:849217-50-1 SDS

849217-50-1Relevant articles and documents

QUINOLYL-CONTAINING COMPOUND AND PHARMACEUTICAL COMPOSITION, AND USE THEREOF

-

, (2022/02/19)

Provided is a quinolyl-containing compound as shown in general formula (I) or (II) or a pharmaceutically acceptable salt, a solvate, an active metabolite, a polymorph, an isotopic label, or an isomer thereof, and further provided are a pharmaceutical composition comprising the compound and use of the compound and the pharmaceutical composition. The provided compound has a dual molecule function, can serve as multi -target inhibitors of novel tyrosine kinase/histone deacetylase, can simultaneously achieve the effect of two inhibitors, has excellent biological activity and pharmacokinetic properties, and has the application potential particularly in the field of treatment of tumors.

Preparation methods of tyrosine kinase inhibitor XJF007 and its intermediate

-

, (2019/07/04)

The invention discloses preparation methods of tyrosine kinase inhibitor XJF007 with a general structural formula (I) and its intermediate. The preparation method of the tyrosine kinase inhibitor XJF007 employs a collecting synthesis strategy of construct

A alkyne generation quinoline derivatives and its preparation and use

-

, (2017/08/25)

The invention discloses alkynylquinoline derivatives, and a preparation method and application thereof. The acetylenoquinoline derivatives are alkynylquinoline compounds as shown in a general formula I which is described in the specification and pharmaceutically acceptable salts, hydrates, solvates and prodrugs thereof. The invention also provides the preparation method for the derivatives and relates to inhibition activity of the compounds as shown in the formula I to a variety of protein tyrosine kinases (e.g. C-Met and VEGFR). Thus, the compounds can be used as anticancer drugs for treatment of human cancers.

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