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6,7-dimethoxy-2,4-dimethylquinazoline is a heterocyclic organic compound characterized by a quinazoline ring structure, which is a fused pyrimidine-benzene ring system. This particular compound features two methyl groups at the 2 and 4 positions of the quinazoline ring and two methoxy groups at the 6 and 7 positions. The presence of these substituents influences the compound's chemical properties, such as solubility and reactivity. It is synthesized through various chemical reactions and is used in the pharmaceutical industry as a potential drug candidate due to its potential biological activities. The compound's structure and functional groups make it a subject of interest for further research in medicinal chemistry and drug development.

4101-17-1

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4101-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4101-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4101-17:
(6*4)+(5*1)+(4*0)+(3*1)+(2*1)+(1*7)=41
41 % 10 = 1
So 4101-17-1 is a valid CAS Registry Number.

4101-17-1Downstream Products

4101-17-1Relevant articles and documents

An Efficient Three-component, One-pot Synthesis of Quinazolines under Solvent-free and Catalyst-free Condition

Bhat, Subrahmanya Ishwar,Das,Trivedi, Darshak R.

, p. 1253 - 1259 (2015)

An efficient green protocol for the synthesis of quinazolines in the absence of solvent and catalyst has been developed. 2,4-Disubstituted quinazolines have been synthesized from three-component one-pot reactions of 2-aminoaryl ketones, orthoesters, and ammonium acetate. The present method has advantages of operational simplicity, substrate generality, clean reaction, high yields (76-94%), and moderate reaction time. The plausible mechanism of the reaction has been proposed based on the spectral characterization and single crystal X-ray analysis of isolated intermediate.

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