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6-fluoro-3-phenyl-2-(trifluoromethyl)quinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49579-40-0

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49579-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49579-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,7 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49579-40:
(7*4)+(6*9)+(5*5)+(4*7)+(3*9)+(2*4)+(1*0)=170
170 % 10 = 0
So 49579-40-0 is a valid CAS Registry Number.

49579-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-3-phenyl-2-(trifluoromethyl)quinazolin-4-one

1.2 Other means of identification

Product number -
Other names -

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:49579-40-0 SDS

49579-40-0Downstream Products

49579-40-0Relevant academic research and scientific papers

Preparation method of 2 -trifluoromethyl-substituted quinazolinone derivative (by machine translation)

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Paragraph 0033-0039; 0042-0048, (2021/01/04)

The invention discloses a preparation method of 2 -trifluoromethyl-substituted quinazolinone derivatives, which comprises the following steps: a palladium catalyst is prepared. Ligands, carbon monoxide alternatives, additives, trifluoroethylimino chloride and o-iodoanilines are added to the organic solvent. Reaction 90 °C was carried out 16 - 30 hours, and after completion of the reaction, the resulting 2 -trifluoromethyl-substituted quinazolinone derivative was obtained. The preparation method is simple and convenient to operate, the reaction starting materials are cheap and easily available, various substituent groups can be compatible, the substrate applicability is good, the substituted trifluoromethyl quinazolinone derivatives with different groups can be synthesized through substrate design, operation is facilitated, and the practicability of the method is widened. To the method, 1,tricarboxylic acid phenol ester is the solid carbon monoxide substitute, has avoided poisonous and colorless gaseous carbon monoxide's use . (by machine translation)

FeCl3-Mediated Synthesis of 2-(Trifluoromethyl)quinazolin-4(3 H)-ones from Isatins and Trifluoroacetimidoyl Chlorides

Wang, Le-Cheng,Du, Shiying,Chen, Zhengkai,Wu, Xiao-Feng

, p. 5567 - 5571 (2020/07/14)

An FeCl3-mediated cascade coupling/decarbonylative annulation reaction for the efficient construction of 2-(trifluoromethyl)quinazolin-4(3H)-ones has been developed. This transformation employs readily available isatins and trifluoroacetimidoyl chlorides as the starting materials, providing a facile and practical route to diverse biologically relevant quinazolin-4(3H)-one derivatives. A plausible reaction pathway has been proposed based on the mechanistic observations.

Preparation method of 2 - trifluoromethyl substituted quinazoline ketone compound (by machine translation)

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Paragraph 0034-0041; 0049-0055, (2020/09/30)

The invention discloses a preparation method of 2 -trifluoromethyl-substituted quinazolone compounds, which comprises the following steps: ferric trichloride and sodium hydrogen. The molecular sieve, trifluoroethyl imine acyl chloride and indirubin were a

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