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2-(4-HYDROXYPHENYL)-1,8-NAPHTHYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65182-55-0

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65182-55-0 Usage

Molecular structure

Contains a naphthyridine core and a hydroxyphenyl group.

Common use

Used as a building block in the synthesis of pharmaceuticals and other organic compounds.

Unique chemical properties

Provided by the hydroxyphenyl group.

Versatility

Allows for use in various chemical reactions and applications.

Importance in development

Molecular structure and properties make it an important component in the development of diverse chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 65182-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65182-55:
(7*6)+(6*5)+(5*1)+(4*8)+(3*2)+(2*5)+(1*5)=130
130 % 10 = 0
So 65182-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O/c17-12-6-3-10(4-7-12)13-8-5-11-2-1-9-15-14(11)16-13/h1-9,17H

65182-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1H-1,8-naphthyridin-2-ylidene)cyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 4-[1,8]naphthyridin-2-yl-phenol

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:65182-55-0 SDS

65182-55-0Downstream Products

65182-55-0Relevant academic research and scientific papers

Microwave assisted synthesis of 1,8- naphthyridines

Mogilaiah,Reddy,Rao

, p. 837 - 838 (2007/10/03)

A highly efficient and practical methodology for the synthesis of 2-aryl-1.8-naphthyridines 3 is described starting from 2-aminonicotinaldehyde 1 and various acetophenones under microwave conditions.

Substituted 1,8-Naphthyridines: Part VI - Synthesis of 3-Aroyl-2-phenyl-1,8-naphthyridines

Rao, G. Rama,Mogilaiah, K.,Reddy, K. Rajendar,Sreenivasulu, B.

, p. 200 - 202 (2007/10/02)

The condensation of 2-aminonicotinaldehyde (1) with ω-benzoylacetophenones (2) leads to either 3-aroyl-2-phenyl-1,8-naphthyridines (3) in the presence of gl. acetic acid containing a catalytic amount of conc.H2SO4, or to 2-aryl-1,8-naphthyridines (4) in e

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