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1147271-25-7

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1147271-25-7 Usage

Chemical Class

Indeno[1,2-d]pyrimidine derivatives

Heterocyclic Core

Indeno[1,2-d]pyrimidine

Functional Groups

Amino group at the 2-position
Morpholinoethoxy group at the 8-position
Phenyl group at the 4-position

Biological Activities

Antitumor: Potential for combating tumors.
Antiviral: Potential for inhibiting viral activity.

Applications

Medicinal Chemistry: Utilized in drug development.

Value

Diverse Biological Activities: Makes it versatile for medicinal applications.
Unique Structure: Offers potential for novel drug development.

Potential Uses

Drug Development: Targeting various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 1147271-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,2,7 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1147271-25:
(9*1)+(8*1)+(7*4)+(6*7)+(5*2)+(4*7)+(3*1)+(2*2)+(1*5)=137
137 % 10 = 7
So 1147271-25-7 is a valid CAS Registry Number.

1147271-25-7SDS

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 2-Amino-8-(2-morpholin-4-yl-ethoxy)-4-phenyl-indeno[1,2-d]pyrimidin-5-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:1147271-25-7 SDS

1147271-25-7Downstream Products

1147271-25-7Relevant articles and documents

Optimization of arylindenopyrimidines as potent adenosine A2A/A1 antagonists

Shook, Brian C.,Rassnick, Stefanie,Chakravarty, Devraj,Wallace, Nathaniel,Ault, Mark,Crooke, Jeffrey,Barbay, J. Kent,Wang, Aihua,Leonard, Kristi,Powell, Mark T.,Alford, Vernon,Hall, Daniel,Rupert, Kenneth C.,Heintzelman, Geoffrey R.,Hansen, Kristen,Bullington, James L.,Scannevin, Robert H.,Carroll, Karen,Lampron, Lisa,Westover, Lori,Russell, Ronald,Branum, Shawn,Wells, Kenneth,Damon, Sandra,Youells, Scott,Beauchamp, Derek,Li, Xun,Rhodes, Kenneth,Jackson, Paul F.

scheme or table, p. 2868 - 2871 (2010/07/06)

Two reactive metabolites were identified in vivo for the dual A2A/A1 receptor antagonist 1. Two strategies were implemented to successfully mitigate the metabolic liabilities associated with 1. Optimization of the arylindenopyrimidines led to a number of amide, ether, and amino analogs having comparable in vitro and in vivo activity.

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