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6-chloro-2-phenyl-4-(2-fluorophenyl)quinazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1283751-57-4

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1283751-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1283751-57-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,7,5 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1283751-57:
(9*1)+(8*2)+(7*8)+(6*3)+(5*7)+(4*5)+(3*1)+(2*5)+(1*7)=174
174 % 10 = 4
So 1283751-57-4 is a valid CAS Registry Number.

1283751-57-4Downstream Products

1283751-57-4Relevant academic research and scientific papers

Lewis-Acid-Catalysed Activation of Nitriles: A Microwave-Assisted Solvent-Free Synthesis of 2,4-Disubstituted Quinazolines and 1,3-Diazaspiro[5.5]undec-1-enes

Saikia, Ujwal Pratim,Borah, Geetika,Pahari, Pallab

supporting information, p. 1211 - 1217 (2018/03/21)

Two different modes of cyclization take place to synthesize quinazoline, quinazolinone, and 1,3-diazaspiro[5.5]undec-1-ene derivatives through the Lewis-acid-catalysed activation of both aliphatic and aromatic nitriles in a single-step, solvent-free, and transition-metal-free reaction. An amidine is expected to form as an intermediate; this then undergoes intramolecular cyclization in a one-pot reaction sequence. The reaction is carried out under microwave irradiation using trimethylsilyltrifluoromethane sulfonate (TMSOTf) as a catalyst and nitriles as a nitrogen source with the respective reaction partners.

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 (2015/08/06)

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.

Microwave-promoted efficient synthesis of dihydroquinazolines

Sarma, Rupam,Prajapati, Dipak

supporting information; experimental part, p. 718 - 722 (2011/05/03)

A solvent- and catalyst-free synthesis of dihydroquinazolines is described. 2,4-Disubstituted-1,2-dihydroquinazolines can be readily obtained from 2-aminobenzophenone and aldehydes under microwave irradiation using urea as an environmentally benign source

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