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6-Methoxyquinazoline is a heterocyclic organic compound with the molecular formula C10H10N2O. It is a derivative of quinazoline, a tricyclic fused aromatic system consisting of a benzene ring fused to a pyrazine ring, with an additional methoxy group attached at the 6th position. 6-Methoxyquinazoline is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the preparation of other organic compounds. 6-Methoxyquinazoline is characterized by its white crystalline appearance and is soluble in common organic solvents. Its chemical properties include reactivity towards electrophilic substitution and nucleophilic addition reactions, making it a versatile building block in organic synthesis.

7556-92-5

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7556-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7556-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7556-92:
(6*7)+(5*5)+(4*5)+(3*6)+(2*9)+(1*2)=125
125 % 10 = 5
So 7556-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-12-8-2-3-9-7(4-8)5-10-6-11-9/h2-6H,1H3

7556-92-5SDS

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 6-Methoxyquinazoline

1.2 Other means of identification

Product number -
Other names 6-(methyloxy)quinazoline

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:7556-92-5 SDS

7556-92-5Downstream Products

7556-92-5Relevant academic research and scientific papers

New method for the direct electrophilic amination of aromatic compounds and its use in the annelation of the pyrimidine ring

Aksenov,Lyakhovnenko,Kugutov

experimental part, p. 1262 - 1265 (2011/10/09)

A method has been developed for the synthesis of aromatic amines by the amination of the corresponding aromatic compounds using sodium azide in PPA. A method for the synthesis of quinazolines and benzo[h]quinazolines using this reaction and the subsequent reaction of the intermediates with 1,3,5-triazines has been developed.

A microwave improvement in the synthesis of the quinazoline scaffold

Chilin, Adriana,Marzaro, Giovanni,Zanatta, Samuele,Guiotto, Adriano

, p. 3229 - 3231 (2008/02/02)

A rapid and efficient microwave-assisted protocol is described that greatly improves a recent synthetic method developed for quinazoline synthesis. The synthetic protocol is based on the use of cycles of microwave irradiation. The optimization process is reported and the experimental results are compared with those of the conventional synthetic route.

A new access to quinazolines from simple anilines

Chilin, Adriana,Marzaro, Giovanni,Zanatta, Samuele,Barbieri, Vera,Pastorini, Giovanni,Manzini, Paolo,Guiotto, Adriano

, p. 12351 - 12356 (2007/10/03)

A new synthetic pathway to quinazolines is described. This new method uses hexamethylenetetramine in TFA and potassium ferricyanide in aqueous ethanolic KOH, starting from simple N-protected anilines. The method affords substituted quinazolines with high

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