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6,7-Dimethoxy-4-methylquinazoline is a heterocyclic organic compound with the molecular formula C11H13N2O2. It features a quinazoline ring, which is a fused pyrimidine-benzene structure, with a methyl group at the 4-position and two methoxy groups at the 6 and 7 positions. 6,7-Dimethoxy-4-methylquinazoline is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as an intermediate in the preparation of compounds with biological activity, such as antitumor, antimicrobial, and antiviral agents. The synthesis of 6,7-dimethoxy-4-methylquinazoline often involves multi-step processes, and its properties, such as solubility and stability, can be influenced by the presence of the methoxy and methyl groups.

4015-31-0

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4015-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4015-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4015-31:
(6*4)+(5*0)+(4*1)+(3*5)+(2*3)+(1*1)=50
50 % 10 = 0
So 4015-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O2/c1-7-8-4-10(14-2)11(15-3)5-9(8)13-6-12-7/h4-6H,1-3H3

4015-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-Dimethoxy-4-methylquinazoline

1.2 Other means of identification

Product number -
Other names 6,7-Dimethoxy-4-methylchinazolin

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:4015-31-0 SDS

4015-31-0Relevant academic research and scientific papers

DIAMINOTHIAZOLES USEFUL AS AXL INHIBITORS

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Page/Page column 49, (2008/12/07)

Diaminothiazoles and pharmaceutical compositions containing them are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the diaminothiazoles in treating diseases or conditions associated with Axl activity are also disclosed.

Synthesis of condensed quinolines and quinazolines as DNA ligands

Malecki, Natacha,Carato, Pascal,Rigo, Benoit,Goossens, Jean-Francois,Houssin, Raymond,Bailly, Christian,Henichart, Jean-Pierre

, p. 641 - 647 (2007/10/03)

Among new condensed quinolines and quinazolines the design of which were inspired by anti-cancer DNA-binding alkaloids such as camptothecin and batracyclin, DNA binding tests identify the 8-methoxy-7- piperazinylpropoxyindeno[1,2-b]quinolin-11-one tetracyclic system as a new motif for DNA recognition.

o-Aminophenyl Alkyl/Aralkyl Ketones and Their Derivatives: Part V -- An Efficient Synthetic Route to Some Biologically Active 4-Substituted Quinazolines

Byford, A.,Goadby, P.,Hooper, M.,Kamath, H. V.,Kulkarni, Sheshgiri N.

, p. 396 - 397 (2007/10/02)

4-Substituted quinazolines (II) have been prepared by the action of formamide on o-aminophenyl alkyl and aralkyl ketones (I) in the presence of borontrifluoride etherate as catalyst, and tested for their inotropic activity.

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