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178548-28-2

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178548-28-2 Usage

Chemical structure

A compound with a naphthyridine core structure and a substituted phenylmethyl group.

Application

Commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals.

Potential uses

Shown potential as an antitumor and anti-inflammatory agent, making it of interest for medicinal chemistry research.

Thermal stability

Exhibits high thermal stability, making it suitable for use in materials science applications.

Chemical nature

Aromatic and heterocyclic, making it a versatile compound for the development of new chemical entities in the field of drug discovery and materials chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 178548-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,5,4 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 178548-28:
(8*1)+(7*7)+(6*8)+(5*5)+(4*4)+(3*8)+(2*2)+(1*8)=182
182 % 10 = 2
So 178548-28-2 is a valid CAS Registry Number.

178548-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-phenyl-1,8-naphthyridin-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:178548-28-2 SDS

178548-28-2Relevant articles and documents

Synthesis of SMP-797: A new potent ACAT inhibitor

Ban, Hitoshi,Muraoka, Masami,Ohashi, Naohito

, p. 10081 - 10092 (2007/10/03)

A potent ACAT (acyl-CoA: cholesterol acyltransferase) inhibitor SMP-797 was effectively synthesized by the urea formation of 3-amino-4-aryl-1,8- naphthyridin-2(1H)-one and 4-amino-2,6-diisopropylamine. The synthesis of the former compound involved the Suzuki coupling reaction as a key step, and the latter was prepared by the 4-selective nitration of 2,6-diisopropylaniline using 2,3,5,6-tetrabromo-4-methyl-4-nitro-2,5-cyclohexadienone.

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